Glossary for Death

Medical terms related to Death or mentioned in this section include:

• $3-$: A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Symptoms tend to be more severe in males who suffer progressive neurodegeneration whereas females tend to suffer mainly from developmental delay.
• $3-Hydroxyisobutyric aciduria$: A rare inborn metabolic disorder which causes brain and facial anomalies, seizures and growth problems.
• $3-alpha-Hydroxyacyl-CoA Dehydrogenase Deficiency$: A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activity prevents some fats being converted into energy. Symptoms tend to be exacerbated during fasting as during fasting, the body tries to rely more heavily on fats for energy. Fatty acids that are not completely metabolized due to the enzyme deficiency may build up in various organs and cause serious complications.
• $3-alpha-hydroxyacyl-coenzyme A dehydrogenase deficiency$: A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activity prevents some fats being converted into energy. Symptoms tend to be exacerbated during fasting as during fasting, the body tries to rely more heavily on fats for energy. Fatty acids that are not completely metabolized due to the enzyme deficiency may build up in various organs and cause serious complications.
• $3-methylglutaconic aciduria, type 1$: A recessively inherited metabolic disorder characterized by methylglutaconic acid in the urine.
• $3-methylglutaconic aciduria, type V$: A rare genetic disorder where the body's cells are unable to make sufficient energy resulting in an accumulation in the body of 3-methylglutaconic acid.
• $4p16.3 deletion$: A rare genetic disorder where a portion of chromosome 4 is deleted at a location called 16.3. The condition is characterized by malformations in most parts of the body as the deletion affects growth and development of the fetus.
• ACAD9 deficiency: A metabolic disorder involving a deficiency of an enzyme (acyl-CoA dehydrogenase-9). The symptoms are variable and are usually triggered by a viral infection or ingestion of aspirin which can trigger a Reye-like episode which can cause death.
• ACE Inhibitors - Teratogenic Agent: There is strong evidence to indicate that the use of ACE Inhibitors during pregnancy may cause a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
• ADANE: A potentially fatal inherited neurological disease involving brain lesions. Symptoms tend to occur during childhood after an illness involving a fever. The disease is similar to Leigh syndrome but the course is acute rather than chronic.
• AIDS-Associated Nephropathy: Kidney disease associated with AIDS.
• AREDYLD: A rare condition characterized by abnormalities of the extremities, teeth, hair, nail and kidney as well as lipoatrophic diabetes.
• Abdominal Injuries: Any injury involving the abdomen. Injuries may penetrating or caused by a fall or blow to the abdomen. Symptoms are variable depending on the nature of the injury.
• Abdominal Neoplasms: A tumor that occurs in the abdomen.
• Abruptio placentae: A condition which is characterized by the premature detachment of the placenta from the uterus
• Abscess: This is an area of puss collected in a cavity which is constituted by necrotised tissue
• Absence of pulmonary artery: The absence of a pulmonary artery at birth.
• Acanthoma: A rare benign or malignant epidermal tumor.
• Accelerated hypertension: Accelerated hypertension is a condition characterized by a rapid increase in blood pressure. The condition is a medical emergency which can cause organ damage if not treated promptly.
• Achondrogenesis type 1A: A rare genetic disorder characterized by abnormal cartilage formation and growth of bones. Type 1A differs from other types by the origin of the genetic defect. Type 1A involves abnormal cartilage-forming cells (chondrocytes) whereas type 1B involves an abnormal cartilage matrix. Type 1B is the most severe disorder.
• Achondrogenesis type 1A and 1B: A rare lethal genetic disorder characterized by a low nasal bridge, very short limbs and incomplete bone formation of lower spine.
• Achondrogenesis type 1B: A rare lethal genetic disorder characterized by a low nasal bridge, very short limbs and incomplete bone formation of lower spine.
• Achondrogenesis type 2: A rare genetic disorder characterized by very small stature, abnormal bone formation and early death.
• Achondrogenesis, Langer-Saldino Type: A rare genetic disorder characterized by very small stature, abnormal bone formation and early death.
• Achondrogenesis, type 3: Severely abnormal bone development which invariably results in death before or soon after birth. Type III may actually be a part of achondrogenesis type II.
• Achrestic anemia: Achrestic anemia is a form of anemia similar to that caused by Vitamin B12 deficiency but it doesn't respond to treatment with Vitamin B12. The condition tends to progress slowly and can result in death if not treated. There are a variety of possible causes.
• Acidemia, methylmalonic: An inborn error of metabolism where amino acids in the body aren't metabolized properly resulting in high levels of the acid throughout the body.
• Acinic cell carcinoma: A usually slow-growing malignant tumor that that can occur in various parts of the body but is most often found in the pancreas, salivary glands, palate and upper lip. Symptoms are determined by the size and location of the growth.
• Ackee Fruit Food poisoning: Unripe ackee fruit contains a chemical called hypoglycin A and B which affect the central nervous system and fatty acid oxidation. Eating the unripe fruit can cause symptoms can occur in as little as two hours but is generally 6 to 48 hours. The ackee fruit is found mainly in Jamaica, West Africa, Central America, Sought Florida, southern California and Hawaii.
• Acquired angioedema: A rare disorder characterized by recurring episodes of swelling of parts of the skin or mucous membranes. Sometimes internal organs may be involved. The disorder occurs in patients with lymphoproliferative or autoimmune disorders which result in the dysfunction of a complex blood protein called C1 inhibitor.
• Acral lentiginous melanoma: Acral lentigous melanoma is the most common variant of skin cancer seen in dark-skinned people. This form of melanoma appears on the palms of the hands, the soles of the feet, or on nails. Lesions are usually brown, black, or multicolored with irregular borders, and flat or nodular.
• Acrofacial dysostosis Preis type: One of a group of disorders characterized by defective limb and facial development. The Preis type is very rare and the range and severity of symptoms is variable.
• Acrofacial dysostosis Rodriguez type: One of a group of disorders characterized by defective limb and facial development. The Rodriguez type is very rare and primarily involves severe limb and organ malformations.
• Acrorenal syndrome recessive: A rare, recessively inherited disorder characterized by the association of kidney and hand and foot abnormalities.
• Acute Bokhoror: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. Death is common in the acute phase of the infection which can last from four days to four months.
• Acute Interstitial Pneumonia: A relatively uncommon form of pneumonia that has no apparent cause. Symptoms tend to develop over a period of six months to one and a half years.
• Acute Silicosis: An occupation lung disease caused by breathing in high levels of silica dust.
• Acute VE: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. Death is common in the acute phase of the infection which can last from four days to four months.
• Acute Viliuisk Encephalitis: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. Death is common in the acute phase of the infection which can last from four days to four months.
• Acute Viliuisk Encephalomyelitis: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. Death is common in the acute phase of the infection which can last from four days to four months.
• Acute Vilyuisk Encephalitis: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. Death is common in the acute phase of the infection which can last from four days to four months.
• Acute Vilyuisk Encephalomyelitis: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. Death is common in the acute phase of the infection which can last from four days to four months.
• Acute adult T-Cell leukemia: A form of blood cancer affecting the T-cells which make up the body's immune system. The disease is caused by the HTLV-1 virus (human T-cell leukemia virus) which causes the proliferation of abnormal T-cells. The virus can be transmitted sexually and may lay dormant for decades. There are four subtypes: acute, chronic, lymphoma and smoldering. The acute and lymphoma subtypes have the poorest prognosis. The acute subtype tends to progress rapidly and is the most prevalent form of the condition.
• Acute appendicitis: Infection of the appendix
• Acute basophilic leukaemia: A rare type of acute myeloid leukemia characterized by the presence of abnormal basophils.
• Acute elemental mercury inhalation: Inhalation of elemental mercury can lead to breathing and lung symptoms of various degrees of severity depending on the level of exposure.
• Acute fatty liver of pregnancy: A rare complication of pregnancy that can occur in the second half of the pregnancy. It is characterized by excessive fatty deposits in the liver which can be fatal without prompt diagnosis and treatment which involves delivering the baby as soon as possible.
• Acute hemorrhagic leukoencephalitis: A rare degenerative brain disease where the patient suffers edema, many small hemorrhages, necrosis of blood vessel walls, demyelination of nerve fibers. Histiocytes, lymphocytes and neutrophils also enter the meninges. Symptoms include severe headache, fever, vomiting and sometimes convulsions and unconsciousness. Also called acute hemorrhagic leukoencephalitis.
• Acute megacaryoblastic leukemia: A rare form of malignant bone marrow cancer involving the proliferation of immature precursors of blood cells. More specifically, it involves the rapid proliferation of megakaryoblasts (premature form of megakaryocytes).
• Acute mercury inhalation: Inhalation of mercury vapor can lead to serious symptoms and even death if sufficient quantities are inhaled. Mercury inhalation is more likely in confined or poorly ventilated spaces. Mercury from a broken thermometer can lead to symptoms if it occurs in a confined space.
• Acute myeloblastic leukemia type 1: A form of blood cancer resulting in the rapid proliferation of immature blood cells (blast cells).
• Acute myelocytic leukemia: A malignant cancer of blood-forming tissues resulting in a high number of immature leukocytes. Symptoms include soft bleeding gums, anemia, fatigue, fever, dyspnea, moderate splenomegaly, joint and bone pains and frequent infections. Also called acute granulocytic leukemia, acute myelogenous leukemia, acute nonlymphocytic leukemia, myeloid leukemia, splenomedullary leukemia, splenomyelogenous leukemia.
• Acute myelofibrosis: A rare condition where progressive scarring or fibrosis of the bone marrow impairs it's ability to make blood cells causing symptoms such as anemia and liver and spleen enlargement.
• Acute myeloid leukaemia and myelodysplastic syndromes related to alkylating agent: The use of alkylating agents to treat cancer can result in leukemia in some patients.
• Acute myeloid leukaemia and myelodysplastic syndromes related to topoisomerase type II inhibitor: The use of topoisomerase type II inhibitors to treat cancer can result in leukemia in some patients.
• Acute myeloid leukaemia and myelodysplastic syndromes, therapy related: Certain cancer therapies can result in the development of leukemia in some patients. These therapies includes topoisomerase type II inhibitors and alkylating agents.
• Acute myeloid leukemia: A form of rapidly progressing blood cancer resulting in the rapid proliferation of granulocytes and monocytes, red blood cells and platelets.
• Acute myelosclerosis: A rare disorder where the bone marrow makes too many blood cells. The disease progresses rapidly with death usually occurring within 6 months of onset.
• Acute pancreatitis: sudden inflammation of the pancreas
• Acute panmyelosis: A rare condition where progressive scarring or fibrosis of the bone marrow impairs it's ability to make blood cells causing symptoms such as anemia and liver and spleen enlargement. The disease often progresses rapidly and results in death.
• Acute panmyelosis with myelofibrosis: A poorly defined condition which is more a description of a particular state rather than a distinct disorder. The condition involves the presence of panmyelosis and myelofibrosis. Bone marrow exposure to toxic substances is one cause of the condition.
• Acute rheumatic fever: Bacterial joint infection with risk of heart complications.
• Adamantinoma: A very aggressive malignant cancer of the jaw. Also called ameloblastoma, adamantoblastoma or epithelioma adamantinum.
• Adducted thumbs - arthrogryposis, Christian type: A rare recessively inherited disorder characterized mainly by a small head, arthrogryposis (joint contractures), cleft palate and various other abnormalities.
• Adenocarcinoid tumor: A rare type of tumor that occurs in the gastrointestinal tract and tends to metastasize. The symptoms are determined by the location of the tumors.
• Adenocarcinoma of lung: A tumor that develops in the lining of the lung. The tumor is usually slow growing.
• Adenocarcinoma, Bronchiolo-Alveolar: A form of lung cancer that develops in the bronchioles or alveoli.
• Adenocarcinoma, Clear Cell: A type of cancer that occurs mainly in the genitourinary tract and the cells that make up the tumor are clear. It is very rare and most cases occur in females whose mothers used a drug called DES (synthetic estrogen) while pregnant.
• Adenocarcinoma, Follicular: A type of cancer of the thyroid gland.
• Adenosarcoma of the uterus: A tumor that develops from the glands that line the uterus.
• Adenosine deaminase deficiency: A rare disorder where a deficiency in the activity of adenosine deaminase causes severe immunodeficiency which in turn results in frequent severe bacterial, viral and fungal infections.
• Adenoviridae Infections: Infection with a virus from the Adenoviridae family. The most common sites for infection are membrane linings such as the intestines, respiratory and urinary tract and the eyes. The infection may result in a range of symptoms depending on the particular virus involved. Transmission usually occurs through breathing in the germs or through fecal-oral contact. The infection is contagious.
• Adenovirus infection in immunocompromised patients: Infection with a virus from the Adenoviridae family that occurs in a patient with a weakened immune system. The infection in these people is serious and can be fatal. The infection may result in a range of symptoms depending on the particular virus involved. Transmission usually occurs through breathing in the germs or through fecal-oral contact.
• Adhesive abuse: Adhesive abuse is the use of various inhalants for the purpose of achieving a "high". They are often used as a cheap, readily available alternative to street drugs but they can cause serious damage to the body. Adhesives include household glues, rubber cement and model aeroplane glue. These adhesives can be abused by sniffing them, spraying directly into the mouth, heating them and then inhaling them or injecting them directly into the body.
• Adhesive addiction: Adhesive addiction refers to the compulsive need to abuse adhesives (e.g. sniffing them). Sufferers have withdrawal symptoms when attempting to stop the habit and feel unable to stop the habit despite knowing the harm it is causing their health. Aerosols are very damaging to the body and can readily result permanent brain damage and even death. Death can occur through chronic use and in rare cases can occur after one session of use. Children and teenagers are particular at risk for this type of addiction - it is readily available and users feel it gains them greater acceptance from their peers. Adhesives includes household glue, rubber cement and model airplane glue.
• Adrenal Cancer: A malignant cancer that develops in the adrenal gland. The tumor may be nonfunctioning (does not produce hormones) or functioning in which case excessive levels of hormones can cause a variety of symptoms depending on which hormone is involved. Adrenal hormones made in the cortex (outer part of the gland) are aldosterone, corticosteroids and androgenic steroids. Adrenalin and noradrenalin are the hormones made in the medulla (central part of the adrenal gland).
• Adrenal Cortex Neoplasms: A tumor that develops in the adrenal gland. The tumor may be nonfunctioning (does not produce hormones) or functioning in which case excessive levels of hormones can cause a variety of symptoms depending on which hormone is involved. Adrenal hormones made in the cortex (outer part of the gland) are aldosterone, corticosteroids and androgenic steroids.
• Adrenal Hyperplasia, Congenital (General): Congenital adrenal hyperplasia is an inherited condition characterized by adrenal insufficiency. It is caused by a deficiency in an enzyme needed to produce certain adrenal hormones such as cortisol and aldosterone.
• Adrenal gland symptoms: Symptoms affecting the adrenal glands
• Adrenal hypertension: Adrenal hypertension is high blood pressure caused by adrenal gland problems. For example, an adrenal tumor can cause excessive production of aldosterone which in turn causes salt-retention and high blood pressure. Severity of symptoms varies depending on the underlying cause.
• Adrenal incidentaloma: A tumor of the adrenal gland that is discovered incidentally while performing an imaging examination for reasons other than an adrenal tumor. The tumor may be asymptomatic or can causes excessive secretion of adrenal hormones and resulting symptoms. The tumor may also be malignant or benign.
• Adrenal medulla neoplasm: A tumor that develops in the part of the adrenal gland called the medulla which produces adrenalin and noradrenaline. The tumor is usually benign but can be malignant.
• Adrenocortical carcinoma: A condition which is characterized by malignancy which affects the adrenocortex.
• Adrenomyeloneuropathy: A form of X-linked adrenoleukodystrophy characterized by spinal cord dysfunction and brain involvement may or may not be present. Those with brain involvement suffer serious symptoms that can eventually lead to total disability and even death.
• Adrenomyodystrophy: A rare genetic disorder characterized by primary adrenal insufficiency, dystrophic myopathy, severe psychomotor retardation and an overly-distended bladder which can cause death.
• Adult T-Cell leukemia: A form of blood cancer affecting the T-cells which make up the body's immune system. The disease is caused by the HTLV-1 virus (human T-cell leukemia virus) which causes the proliferation of abnormal T-cells. The virus can be transmitted sexually and may lay dormant for decades. There are four subtypes: acute, chronic, lymphoma and smoldering. The acute and lymphoma subtypes have the poorest prognosis.
• Adult T-Cell lymphoma: A form of blood cancer affecting the T-cells which make up the body's immune system. The disease is caused by the HTLV-1 virus (human T-cell leukemia virus) which causes the proliferation of abnormal T-cells. The virus can be transmitted sexually and may lay dormant for decades. There are four subtypes: acute, chronic, lymphoma and smoldering. The acute and lymphoma subtypes have the poorest prognosis. The lymphoma subtype is aggressive and tends to affect the lymph nodes more than the blood.
• Adult respiratory distress syndrome: A condition which is characterized by fulminant pulmonary interstitial alveolar oedema.
• Adult-onset asthma: Adult-onset asthma is a type of asthma that occurs during adulthood. Asthma involves constriction and inflammation of the airways. The severity of symptoms is variable. Allergies account for about half the cases of adult-onset asthma.
• Aerosol abuse: Aerosol abuse is the use of various inhalants for the purpose of achieving a "high". They are often used as a cheap, readily available alternative to street drugs but they can cause serious damage to the body. Aerosols include air fresheners, hair spray, spray pain and deodorants. These aerosols can be abused by sniffing them, spraying directly into the mouth, heating them and then inhaling them or injecting them directly into the body.
• Aerosol addiction: Aerosol addiction refers to the compulsive need to abuse aerosol (e.g. sniffing them). Sufferers have withdrawal symptoms when attempting to stop the habit and feel unable to stop the habit despite knowing the harm it is causing their health. Aerosols are very damaging to the body and can readily result permanent brain damage and even death. Death can occur through chronic use and in rare cases can occur after one session of use. Children and teenagers are particular at risk for this type of addiction - it is readily available and users feel it gains them greater acceptance from their peers. Aerosols includes spray pain, air freshener, deodorants and hair sprays.
• Aflatoxin B1 exposure: Aflatoxin B1 is a toxin produced by fungus from the Aspergillus genus. The toxin is carcinogenic in humans and can also cause other health effect, particularly liver problems. The fungus are found frequently in nature and can readily contaminate crops before harvest or during storage. It is common in moist soils and decaying vegetation. There are more than 13 different subtypes of aflatoxin with B1 being the most toxic. The condition is most common in poorly developed countries where there are insufficient controls on the presence of aflatoxin in food.
• Aflatoxin B2 exposure: Aflatoxin B2 is a toxin produced by fungus from the Aspergillus genus. The toxin is carcinogenic in humans and can also cause other health effect, particularly liver problems. The fungus are found frequently in nature and can readily contaminate crops before harvest or during storage. It is common in moist soils and decaying vegetation. There are more than 13 different subtypes of aflatoxin with B1 being the most toxic. The condition is most common in poorly developed countries where there are insufficient controls on the presence of aflatoxin in food.
• Aflatoxin G1 exposure: Aflatoxin G1 is a toxin produced by fungus from the Aspergillus genus. The toxin is carcinogenic in humans and can also cause other health effect, particularly liver problems. The fungus are found frequently in nature and can readily contaminate crops before harvest or during storage. It is common in moist soils and decaying vegetation. There are more than 13 different subtypes of aflatoxin with B1 being the most toxic. The condition is most common in poorly developed countries where there are insufficient controls on the presence of aflatoxin in food.
• Aflatoxin G2 exposure: Aflatoxin G2 is a toxin produced by fungus from the Aspergillus genus. The toxin is carcinogenic in humans and can also cause other health effect, particularly liver problems. The fungus are found frequently in nature and can readily contaminate crops before harvest or during storage. It is common in moist soils and decaying vegetation. There are more than 13 different subtypes of aflatoxin with B1 being the most toxic. The condition is most common in poorly developed countries where there are insufficient controls on the presence of aflatoxin in food.
• Aflatoxin exposure: Aflatoxins are toxins produced by fungus from the Aspergillus genus. The toxin is carcinogenic in humans and can also cause other health effect, particularly liver problems. The fungus are found frequently in nature and can readily contaminate crops before harvest or during storage. It is common in moist soils and decaying vegetation. There are more than 13 different subtypes of aflatoxin with B1 being the most toxic. The condition is most common in poorly developed countries where there are insufficient controls on the presence of aflatoxin in food.
• African Sleeping sickness: A disease caused by parasites (Trypanosome brucei gamiense or T. brucei rodesiense) and transmitted to humans by the tsetse fly which is found only in Africa. Causes symptoms such as fever, chills, headache, anemia, edema of hands and feet, enlarged lymph glands, lethargy, sleepiness, convulsions and coma. Also called African trypanosomiasis and sleeping sickness.
• Aggressive systemic mastocytosis: The excessive proliferation of mast cells. Mast cells control the skin's response to minor injury and release a chemical called histamine which causes the skin to redden. In the aggressive form, mast cells accumulate in the liver, spleen and lymphatic system.
• Agnathia-holoprosencephaly-situs inversus: A very rare disorder characterized by a small or absent jaw, developmental brain defect and internal organs situated on the wrong side of the body (situs inversus). The severity and range of symptoms is variable.
• Aicardi-Goutieres syndrome: A rare inherited progressive disease that affects the brain and immune system.
• Aicardi-Goutieres syndrome 1: A rare inherited progressive disease that affects the brain and immune system. Type 1 is caused by a defect on chromosome 3p21.3-p21.2.
• Aicardi-Goutieres syndrome 2: A rare inherited progressive disease that affects the brain and immune system. Type 2 is caused by a defect on chromosome 13q14-q21.
• Aicardi-Goutieres syndrome 3: A rare inherited progressive disease that affects the brain and immune system. Type 3 is caused by a defect on chromosome 11q13.2.
• Aicardi-Goutieres syndrome 4: A rare inherited progressive disease that affects the brain and immune system. Type 4 is caused by a defect on chromosome 19p13.13.
• Aicardi-Goutieres syndrome 5: A rare inherited progressive disease that affects the brain and immune system. Type 5 is caused by a defect on chromosome 3p21.3-p21.2.
• Airway obstruction: airway obstruction is a blockage of the upper airway, which can be in the trachea, laryngeal (voice box), or pharyngeal (throat) areas or involve the bronch.
• Al Gazali Hirschsprung syndrome: A rare disorder characterized by Hirschsprung disease (an intestinal disorder), nail abnormalities and facial anomalies.
• Al Murrah-induced lead poisoning: Al Murrah is a folk remedy used mainly by Saudi Arabian people to treat problems such as stomach pain, diarrhea and colic. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Alarcon-induced lead poisoning: Alarcon is a folk remedy used mainly by Mexican people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Albayaidle-induced lead poisoning: Albayaidle is a folk remedy used mainly by Mexican and Central American people to treat digestive or stomach problems such as vomiting and colic. It is also used to treat apathy and lethargy. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Albayalde-induced lead poisoning: Albayalde is a folk remedy used mainly by Mexican and Central American people to treat digestive or stomach problems such as vomiting and colic. It is also used to treat apathy and lethargy. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Albers-Schonberg disease - malignant recessive form: A rare disorder characterized primarily by increased bone density as old bone is not resorbed and replaced with new bone - is also known as marble bone disease. The malignant infantile form is the most severe form of this disorder and death usually occurs in the first decade of life.
• Alcohol abuse: Excessive alcohol as a symptom of other conditions
• Alcohol drinking: The consumption of a drink containing alcohol. Alcohol consumption can cause varying degrees of impairment depending on the amount consumed. Consuming very large amounts of alcohol can lead to death.
• Alcohol-Induced Disorders: Disorders caused by excessive alcohol consumption. The symptoms are variable depending on the disorder involved. Some of the disorders are: alcohol abuse, alcohol dependence, alcohol intoxication, alcohol withdrawal, alcohol intoxication delirium, alcohol withdrawal delirium, alcohol-induced persisting dementia, alcohol-induced persisting amnestic disorder, alcohol-induced psychotic disorder, alcohol-induced mood disorder, alcohol-induced anxiety disorder, alcohol-induced sexual dysfunction, alcohol-induced sleep disorder, liver damage, liver cancer and esophageal cancer.
• Alcohol-induced hypertension: Alcohol-induced hypertension is high blood pressure caused by excessive drinking of alcohol.
• Alcoholic intoxication: The excessive consumption of alcohol can have toxic effects on the body and can ultimately result in death in severe cases.
• Alcoholic liver disease: Alcoholic liver disease is the major cause of liver disease in Western countries, (in Asian countries, viral hepatitis is the major cause). It arises from the excessive ingestion of alcohol.
• Allergic asthma: A form of asthma caused by inhalation of airborne allergenic substance.
• Alopecia - hypogonadism - extrapyramidal disorder: A rare syndrome characterized by alopecia, progressive movement problems and a lack of gonadal function which affects puberty.
• Alpha thalassemia: Thalassemia is an inherited blood disorder characterized by abnormal synthesis of hemoglobin. Hemoglobin consists of two main protein chains called ? and ?. Alpha thalassemia involves defects in one or more of the four genes required to make each ? protein chain. The main symptom is anemia, the severity of which can vary amongst patients depending on how many defective genes are involved.
• Alpha-ketoglutarate dehydrogenase deficiency: A metabolic disorder characterized by a deficiency of Alpha-ketoglutarate dehydrogenase which results in high levels of oxoglutaric acid in the urine as well as other severe symptoms.
• Alveolar Hydatid Disease: Rare multi-organ tapeworm infection caught from animals.
• Alveolar capillary dysplasia: The abnormal development of the lung blood vessels. The normal barrier across which air and blood can diffuse fails to develop properly. Death usually results within weeks of birth but rare cases can survive for months.
• Alzheimer disease 3, (early-onset Alzheimer disease): Alzheimer disease 3 is an early-onset form of Alzheimer's disease that is linked to a defect on chromosome 14q24.3. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
• Alzheimer disease, familial, 3, with spastic paraparesis and apraxia: This form of Alzheimer's is an early-onset form of Alzheimer's that is linked to a defect on chromosome 14q24.3. It is characterized by features which are atypical for Alzheimer's - spastic paraparesis which occurs before the dementia symptoms and apraxia. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
• Alzheimer disease, familial, 3, with spastic paraparesis and unusual plaques: This form of Alzheimer's is an early-onset form of Alzheimer's that is linked to a defect on chromosome 14q24.3. It is characterized by features which are atypical for Alzheimer's - spastic paraparesis which occurs before the dementia symptoms and unusual plaques in the brain. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
• Amanita polypyramis poisoning: Amanita polypyramis is a type of large-capped mushroom often found growing in the wild in the US. The mushroom tends to give off a chlorine-like odor. It is poisonous and death can result if sufficient quantities are eaten.
• Ambien overdose: Ambien is a prescription drug mainly used to treat insomnia. Excessive doses of the drug can result in various symptoms and even death in severe cases.
• Amelia, autosomal recessive: A rare disorder characterized by the complete absence of the arms and a partial absence of the legs. The disorder has been described in the 3 fetuses of one family.
• Aminoacidopathies: Any of a group of inborn errors of metabolism which results in the build up in the body of one or more amino acids in the blood and/or urine. The range and severity of symptoms is hugely variable.
• Amnesic shellfish poisoning: Rare shellfish poisoning sometimes causing amnesia.
• Amniotic fluid syndrome: A rare disorder where large amounts of amniotic fluid suddenly enters the blood stream. The amniotic fluid contains debris which can block blood vessels and dilutes the blood which affects coagulation. This can occur when there is an opening in a blood vessel wall and can occur if the birth involves difficult labor, older women, dead fetus syndrome or large babies. The condition can result in rapid death of the mother.
• Amphetamine abuse: Use of the stimulant drugs known as amphetamines or "speed"
• Amphetamine-induced hypertension: Amphetamine-induced hypertension is high blood pressure caused by use of amphetamines. Patients with an existing history of hypertension may suffer further blood pressure increases while taking amphetamines and this can be serious. Severity of symptoms varies amongst patients depending on their susceptibility, underlying health and duration of amphetamine use.
• Amyloid cardiopathy: Amyloidosis is a rare group of metabolic disorders where a protein called amyloid accumulates in body organs and tissues where it can cause damage and is potentially fatal. The cardiac form involves deposits of amyloid in the heart muscle which affects its function. The electrical conduction system of the heart is impaired.
• Amyotrophic lateral sclerosis-parkinsonism-dementia complex: A nerve degeneration disorder that involves progressive dementia and parkinsonism which ultimately leads to death.
• Amyotrophic lateral sclerosis-parkinsonism/dementia complex 2: A nerve degeneration disorder that involves progressive dementia and parkinsonism which ultimately leads to death.
• Anal cancer: A cancerous malignancy that is located anatomically in the anus
• Anaphylaxis: An immediate hypersensitivity reaction due to the exposure of a specific antigen to a sensitized individual
• Anaplastic large cell lymphoma: A rare type of cancer where a tumor develops in lymph tissue and usually consists of white blood cells and null cells. It is a form of non-Hodgkin's lymphoma. The tumors can develop in more than one lymph node and can also occur in the skin and various organs such as the liver, bones or lungs.
• Anaplastic small cell lymphoma: A rare type of cancer where a tumor develops in lymph tissue and consists mainly of small cells. It is a form of non-Hodgkin's lymphoma. The tumors can develop in more than one lymph node and can also occur in the skin and various organs such as the liver, bones or lungs.
• Anchovy poisoning (clupeotoxin): Some anchovies contain toxins (Clupeotoxin) which can be poisonous to humans if eaten. Heat does not destroy the toxin and there is still uncertainty as to the origin of the toxin. The toxin appears to be present in higher concentrations in summer and is believed to be possible linked to the consumption of toxic food in its food web. The size and age of the anchovy does not appear to be related to the toxicity. The anchovies are found in coastal waters off Africa and the Caribbean, Indian and Pacific Oceans.
• Andrade's syndrome: An inherited condition characterized by deposits of an abnormal protein called amyloid in various parts of the body including organs. The condition mainly involves neurological symptoms.
• Anemia of pregnancy: Anemia of pregnancy is anemia that occurs during pregnancy. Women's bodies have a greater demand for iron during pregnancy and if intake is not sufficient, anemia can result. Anemia in pregnant women can lead to infant problems such as premature birth, fetal death, retarded growth and other problems.
• Anemia, Blackfan Diamond: Diamond-Blackfan anemia is a rare genetic condition where the bone marrow is unable to make sufficient red blood cells which leads low levels of red blood cells. There are eight subtypes of the condition which differ in the location of the genetic defect and the incidence of additional symptoms such as malformations. The severity of symptoms is variable but most cases are serious.
• Anemia, Hemolytic, Warm Antibody: A rare autoimmune condition where the body's defense system attacks and destroys red blood cells. The onset of the condition is triggered by temperatures 37ºC or higher. The severity of the disorder is variable.
• Anemia, Refractory, with Excess of Blasts: A bone marrow disease which results in insufficient red blood cells in the blood (anemia). The prognosis is poor with death usually occurring within a couple of years. There are two types: type 1 refers to cases where the level of blasts is less than 10% and type 2 refers to cases where the level of blasts is 10-20%. When too many immature blood cells (blasts) are produced by the bone marrow, the condition may progress to acute myeloid leukemia - occurs in about a quarter of cases in type 1 and a third of cases in type 2.
• Anemia, Refractory, with Excess of Blasts, type 1: A bone marrow disease which results in insufficient red blood cells in the blood (anemia). The prognosis is poor with death usually occurring within a couple of years. Type 1 refers to cases where the level of blasts is less than 10% and type 2 refers to cases where the level of blasts is 10-20%. When too many immature blood cells (blasts) are produced by the bone marrow, the condition may progress to acute myeloid leukemia - occurs in about a quarter of cases in type 1.
• Anemia, Refractory, with Excess of Blasts, type 2: A bone marrow disease which results in insufficient red blood cells in the blood (anemia). The prognosis is poor with death usually occurring within a couple of years. Type 1 refers to cases where the level of blasts is less than 10% and type 2 refers to cases where the level of blasts is 10-20%. When too many immature blood cells (blasts) are produced by the bone marrow, the condition may progress to acute myeloid leukemia - occurs in about a third of cases in type 2.
• Anencephaly: A birth defect where large parts of the brain is missing and the brainstem is malformed.
• Anencephaly and spina bifida X-linked: A severe X-linked malformation syndrome involving anencephaly where a part or all of the brain and associated skull is missing as well as a defect or opening in the spinal column.
• Aneurysm: Swelling or ballooning of part of an artery
• Aneurysm of sinus of Valsalva: A rare form of aortic aneurysm that occurs in the sinus of Valsalva. An aneurysm is a thinning and bulging of a blood vessel wall. The condition is generally asymptomatic unless it burst and causes life-threatening complications including heart failure. An unruptured aneurysm may affect the blood flow (causing palpitations and syncope) as the bulge pushes against surrounding structures.
• Aneurysm, Dissecting: A tear that develops in a part of the aortic blood vessel wall. The three layers of the blood vessel wall separate and cause it to weaken and the aorta to dilate. The condition is fatal if untreated as the weak spot can burst resulting in a hemorrhage.
• Aneurysm, intracranial berry: A bulge in a blood vessel in the brain. The bulge can rupture causing a stroke. They usually form as a result of high blood pressure and weak blood vessel walls in the brain. There are five different subtypes of intracranial berry aneurysms with each one caused by a defect in different gene. The defective gene increases and individuals risk for developing intracranial berry aneurysms.
• Aneurysm, intracranial berry, 1: A bulge in a blood vessel in the brain. The bulge can rupture causing a stroke. They usually form as a result of high blood pressure and weak blood vessel walls in the brain. There are five different subtypes of intracranial berry aneurysms with each one caused by a defect in different gene. The defective gene increases and individuals risk for developing intracranial berry aneurysms. Type 1 is caused by a defect on chromosome 7q11.2.
• Aneurysm, intracranial berry, 2: A bulge in a blood vessel in the brain. The bulge can rupture causing a stroke. They usually form as a result of high blood pressure and weak blood vessel walls in the brain. There are five different subtypes of intracranial berry aneurysms with each one caused by a defect in different gene. The defective gene increases and individuals risk for developing intracranial berry aneurysms. Type 2 is caused by a defect on chromosome 19q13.
• Aneurysm, intracranial berry, 3: A bulge in a blood vessel in the brain. The bulge can rupture causing a stroke. They usually form as a result of high blood pressure and weak blood vessel walls in the brain. There are five different subtypes of intracranial berry aneurysms with each one caused by a defect in different gene. The defective gene increases and individuals risk for developing intracranial berry aneurysms. Type 3 is caused by a defect on chromosome 1p36.13-p34.3.
• Aneurysm, intracranial berry, 4: A bulge in a blood vessel in the brain. The bulge can rupture causing a stroke. They usually form as a result of high blood pressure and weak blood vessel walls in the brain. There are five different subtypes of intracranial berry aneurysms with each one caused by a defect in different gene. The defective gene increases and individuals risk for developing intracranial berry aneurysms. Type 4 is caused by a defect on chromosome 5p15.2-14.3.
• Aneurysm, intracranial berry, 5: A bulge in a blood vessel in the brain. The bulge can rupture causing a stroke. They usually form as a result of high blood pressure and weak blood vessel walls in the brain. There are five different subtypes of intracranial berry aneurysms with each one caused by a defect in different gene. The defective gene increases and individuals risk for developing intracranial berry aneurysms. Type 5 is caused by a defect on chromosome 2p13.
• Aneurysm, intracranial berry, 6: A bulge in a blood vessel in the brain. The bulge can rupture causing a stroke. They usually form as a result of high blood pressure and weak blood vessel walls in the brain. There are now six different subtypes of intracranial berry aneurysms with each one caused by a defect in different gene. The defective gene increases an individuals risk for developing intracranial berry aneurysms. Type 6 is caused by a defect on chromosome 9p21.
• Aneurysm, intracranial berry, 7: A bulge in a blood vessel in the brain. The bulge can rupture causing a stroke. They usually form as a result of high blood pressure and weak blood vessel walls in the brain. There are five different subtypes of intracranial berry aneurysms with each one caused by a defect in different gene. The defective gene increases and individuals risk for developing intracranial berry aneurysms. Type 7 is caused by a defect on chromosome 11q24-q25.
• Aneurysm, intracranial berry, 8: A bulge in a blood vessel in the brain. The bulge can rupture causing a stroke. They usually form as a result of high blood pressure and weak blood vessel walls in the brain. There are five different subtypes of intracranial berry aneurysms with each one caused by a defect in different gene. The defective gene increases and individuals risk for developing intracranial berry aneurysms. Type 8 is caused by a defect on chromosome 14q23.
• Aneurysmal subarachnoid haemorrhage: Bleeding in the space around the brain that occurs from a leak in a weakened or dilated blood vessel under the arachnoid layer of the brain. Death can occur if treatment is not prompt.
• Angiosarcoma: A rare, aggressive malignant tumor of the blood vessel cells. Also called hemangiosarcoma, malignant hemangioendothelioma.
• Angiosarcoma of the breast: A rare type of cancer that starts in the lining of blood vessels in the breast. It is generally an aggressive tumor which often metastasizes.
• Angiosarcoma of the liver: A rare type of cancer that starts in the lining of blood vessels in the liver. It is generally an aggressive tumor which often metastasizes.
• Angiosarcoma of the scalp: A rare type of cancer that starts in the lining of blood vessels in the scalp. It is generally an aggressive tumor which often metastasizes.
• Anguillulosis: A infectious disease caused by an intestinal parasite called Strongyloides stercoralis (round worm). Infestation can occur directly through broken skin or through ingestion. Symptoms can take decades to develop in some cases. In rare cases, reinfection occurs and the parasites travel to other parts of the body such as the liver and lungs which can cause serious symptoms. The condition is highly deadly in immunocompromised patients.
• Anophthalmia - hypothalamo-pituitary insufficiency: A rare syndrome characterized mainly by small or absent eyes and malformations of the hypothalamus and pituitary gland.
• Anophthalmia - hypyothalamo-pituitary insufficiency: A rare syndrome characterized mainly by small or absent eyes and malformations of the hypothalamus and pituitary gland.
• Anophthalmia with pulmonary hypoplasia: A rare disorder characterized by absent or very small eyes and underdeveloped lung tissue.
• Anorectal atresia: Congenital malformation where the anal or rectal opening is obstructed. The malformation is often associated with other abnormalities.
• Anorexia Nervosa: A disorder where a distorted sense of body image leads to self-starvation to the point of death in some cases.
• Anoxemia: Lack of oxygen in the blood.
• Antepartum Eclampsia: Antepartum eclampsia is the development of seizures or coma in pregnant women suffering from high blood pressure. Antepartum means that it occurs before delivery. Eclampsia is a serious condition which requires urgent medical treatment. Eclampsia may be associated with moderate as well as significant increases in blood pressure. The blood pressure can return to normal after delivery or may persist for a period of time.
• Anthrax: A serious infectious bacterial disease that can be fatal.
• Antihypertensive drug allergy: Taking antihypertensive drugs (blood pressure-lowering drugs) can cause an allergic response in some people however this is considered rare. It involves the body's immune system overreacting to the drug. The type and severity of symptoms can vary considerable though skin symptoms are the most common allergic response to drugs.
• Antiphospholipid syndrome: An autoimmune disorder characterized by blood clots and pregnancy losses.
• Aortic Aneurysm, Thoracic: Bulging and weakness of the aorta in the area of the chest. The condition is life-threatening as death can occur rapidly if the aneurysm bursts.
• Aortic aneurysm, familial abdominal 1: A rare familial disorder where the abdominal aorta has a weak, bulging portion. The condition is asymptomatic but can result in death if it bursts. Type 1 is caused by a genetic defect on chromosome 19q13.
• Aortic aneurysm, familial abdominal 2: A rare familial disorder where the abdominal aorta has a weak, bulging portion. The condition is asymptomatic but can result in death if it bursts. Type 2 is caused by a genetic defect on chromosome 4q31.
• Aortic aneurysm, familial abdominal 3: A rare familial disorder where the abdominal aorta has a weak, bulging portion. The condition is asymptomatic but can result in death if it bursts. Type 3 is caused by a genetic defect on chromosome 9p21.
• Aortic aneurysm, familial thoracic 1: A rare familial disorder where the aorta has a weak, bulging portion. The condition is asymptomatic but can result in death if it bursts. Type 1 is caused by a genetic defect on chromosome 11q23.3-q24.
• Aortic aneurysm, familial thoracic 2: A rare familial disorder where the aorta has a weak, bulging portion. The condition is asymptomatic but can result in death if it bursts. Type 2 is caused by a genetic defect on chromosome 5q13-q14.
• Aortic aneurysm, familial thoracic 3: A rare familial disorder where the aorta has a weak, bulging portion. The condition is asymptomatic but can result in death if it bursts. Type 3 is caused by a genetic defect on chromosome 3p22.
• Aortic aneurysm, familial thoracic 4: A rare familial disorder where the aorta has a weak, bulging portion. The condition is asymptomatic but can result in death if it bursts. Type 4 also involves another heart defect (patent ductus arteriosus) and is caused by a genetic defect on chromosome 16p13.13-p13.12.
• Aortic aneurysm, familial thoracic 5: A rare familial disorder where the aorta has a weak, bulging portion. The condition is asymptomatic but can result in death if it bursts. Type 5 is caused by a genetic defect on chromosome 9q33-q34.
• Aortic arch interruption: A rare genetic birth defect where a portion of the aortic arch is missing or discontinued which severely impairs the flow of oxygenated blood to the lower body.
• Aortic arches defect: A defect in the top part of the aorta (aortic arch) that consists of several arterial branches. There is a variety of defects that can occur and symptoms will be determined by the particular defect involved. Possible types of defects includes aortic coarctation and aortic arch hypoplasia.
• Aortic coarctation: A rare inherited birth defect where the heart blood vessel called the aorta has a narrowed area which affects blood flow. The degree of constriction is variable which mild cases asymptomatic until adulthood. The poor blood flow to the lower body gives results in it appearing less developed than that upper body.
• Aorto-ventricular tunnel: A rare heart defect where a tunnel from between the ascending aorta and the cavity of the left or sometimes right heart ventricle. The severity of the condition is highly variable from asymptomatic for many years to fetal death. Often other heart anomalies are also associated.
• Apnea: Periods of absence of breathing
• Apnea of infancy (AOI): Temporary cessation of breathing in infants (under one year old) for longer than 15-20 seconds. The infants are not premature.
• Appendiceal tumor: A tumor of the appendix. The condition is often misdiagnosed as acute appendicitis. The cancer usually metastasizes from other sites and rarely starts in the appendix.
• Appendix cancer: Cancer of the appendix. The cancer usually metastasizes from other sites and rarely starts in the appendix.
• Appian-Plutarch syndrome: Symptoms caused by excessive doses of a drug called atropine.
• Apple seed poisoning: Apple seeds contain a toxic chemical called amygdalin which can cause serious symptoms if eaten in large quantities. Hospital admission is recommended if more than 50 apple seeds have been consumed.
• Apricot seed poisoning: Apricot seeds contain a chemical called amygdalin which breaks down into cyanide in the human body. The toxic chemicals are not released if the pit remains intact and therefore poisoning usually occurs if the seeds are crushed and eaten. Accidental ingestion is very unusual. Most parts of the apricot plant contain the toxic chemical with the highest concentration in young leaves. Different species of apricots have different levels of toxic chemical. Severe symptoms or even death can occur if children consume more than ten kernels or adults consume more than forty kernels. Theories exist that apricot kernels may help cancer sufferers but there has been no scientific studies that have proven this.
• Arachnidism: Poisoning from a spider bite.
• Arbovirosis: An infectious disease caused by an arbovirus. The virus is transmitted by arthropods such as insects and ticks. Examples of arboviruses include Yellow Fever, Japanese encephalitis and tick-borne encephalitis. The symptoms may vary depending on the type of virus involved. The infection can lead to life-threatening brain inflammation.
• Arcobacter butzleri infection: A bacterial infection that involves bacteria from the Arcobacter genus. It tends to cause gastrointestinal symptoms but may also cause blood infections. The bacteria tends to originate in pigs, cattle, sheep and water.
• Arcobacter cryaerophilus infection: A bacterial infection that involves bacteria from the Arcobacter genus. It tends to cause gastrointestinal symptoms but may also cause blood infections. The bacteria tends to originate in pigs, cattle, sheep and water.
• Arcobacter infection: A bacterial infection that involves bacteria from the Arcobacter genus. It tends to cause gastrointestinal symptoms but may also cause blood infections. The bacteria tends to originate in pigs, cattle, sheep and water.
• Arctic bearded seal poisoning: The Arctic Bearded seal is often used as a food source by the arctic inhabitants. Eating the liver and kidneys of the arctic bearded seal can result in a Vitamin A overdose which can cause serious symptoms and even death in extreme cases. It is believed that eating more than 100-250 grams of the seal liver can result in human death.
• Argentinean hemorrhagic fever: An infectious disease caused by the Junin virus. Transmission can occur through contact with infected rodent (usually the corn mouse) urine, feces or saliva. The incubation period lasts from one to two weeks. The disease is most common in rural workers in Argentina.
• Arginase deficiency: A very rare urea cycle disorder caused by a deficiency of the enzyme (arginase) needed to convert ammonia to the urea which can then be removed in the urine. The condition leads to excess build-up of ammonia in the body which is toxic to the nervous system.
• Aristolochic Acid poisoning: Aristolochic acid is derived from a forest herb from the Aristocholochia family. It is often used in herbal preparations such as Aristolochia Fang Ch, Bragantia and Asarum. It is usually used in herbal preparations to promote weight loss. The substance is believed to cause kidney failure and urinary tract cancer.
• Arizona Bark Scorpion poisoning: A bite from the Arizona Bark scorpion contains chemicals toxic to the nerve system and can cause serious, life-threatening symptoms.
• Arnold-Chiari Malformation (Type 1): A rare malformation where the base of the brain enters into the upper spinal canal.
• Arnold-Chiari malformation type 2: A rare malformation where the base of the brain enters into the upper spinal canal. The extent of the deformity is greater in type 2 than type 1 and hence the symptoms are more severe and are often associated with a myelomeningocele (opening of the spine and spinal cord).
• Arnold-Chiari malformation type 3: An extremely rare malformation where the base of the brain enters into the upper spinal canal. Type 3 involves the herniation of brain or brain stem tissue out of the back of the neck or head. The condition generally has a poor prognosis.
• Arnold-Chiari malformation type 4: Arnold-Chiari malformation is a rare malformation where the base of the brain enters into the upper spinal canal. Type 4 actually involves a lack of development of a portion of the base of the brain (cerebellum). The prognosis is very poor with death often occurring during infancy.
• Arterial calcification of infancy: A rare disorder involving widespread calcification of arteries which obstructs blood flow.
• Arterial dissections with lentiginosis: A rare familial syndrome characterized by the association of aortic dissection and multiple lentigines (brown skin spots). The aorta can rupture in some cases and result in sudden death.
• Arteriosclerosis Obliterans: Arteriosclerosis that results in the narrowing and gradual blockage of the artery. Arteriosclerosis involves the deposition of cholesterol plaques and other material on the inside of the artery walls. The symptoms will depend on the location of the arteries affected and how severe the blockage is.
• Arthrogryposis - renal dysfunction - cholestasis syndrome: A very rare syndrome characterized by joint contractures, kidney dysfunction and liver problems.
• Arthrogryposis due to muscular dystrophy: A rare disorder where a non-progressive muscle disease results in the presence of multiple joint contractures at birth.
• Asherson syndrome: The failure of a muscle at the top of the esophagus to relax and allow food and liquid to pass through. Liquid and even food may accidentally be inhaled and can lead to pneumonia and death in some cases.
• Asiatic porpoise poisoning: The Asiatic porpoise is eaten mainly in China. Eating the liver, internal organs and muscle tissue of the Asiatic porpoise can cause poisoning symptoms in humans if sufficient quantities are consumed. The nature of the toxin is unknown but it is believed that some cases result from very high levels of vitamin A in the liver.
• Aspartylglucosaminidase deficiency: A rare glycoprotein metabolism disorder caused by a deficiency of an enzyme called aspartylglucosaminidase. Patients tend to develop normally during the first few years of life and development continues slowly until adolescence when mental retardation becomes progressively worse.
• Aspartylglucosaminuria: A rare glycoprotein metabolism disorder caused by a deficiency of an enzyme called aspartylglucosaminidase. Patients tend to develop normally during the first few years of life and development continues slowly until adolescence when mental retardation becomes progressively worse.
• Aspartylglycosaminuria: A rare glycoprotein metabolism disorder caused by a deficiency of an enzyme called aspartylglucosaminidase. Patients tend to develop normally during the first few years of life and development continues slowly until adolescence when mental retardation becomes progressively worse.
• Asphyxia neonatorum: Respiratory failure in a newborn.
• Aspirin-induced asthma: Aspirin-induced asthma refers to inflammation and constriction of the airways that is triggered by the use of aspirin. A significant number of patients with aspirin-induced asthma also have steroid-dependant asthma where they require regular steroidal asthma medication to maintain normal lung functioning. The severity of symptoms is variable.
• Asthma: A condition which is characterized by recurrent attacks of paroxysmal dyspnoea
• Asthma in pregnancy: Asthma in pregnancy refers to inflammation and constriction of the airways that is occurs during pregnancy. Women who are pregnancy may decide to stop taking their asthma medication in order to reduce the perceived risk of side effects to the developing fetus. The reality is that the potential harmful effects on the fetus are very small compared to the problems caused to mother and fetus if a severe asthma attack develops. Furthermore, uncontrolled asthma during pregnancy may also cause problems such as small birth weight or premature birth. Pregnant women should consult their physician in order to determine the optimal management of their condition. During pregnancy, asthma symptoms may become worse, improve or stay the same.
• Astley-Kendall syndrome: A very rare syndrome involving abnormal skeletal development and resulting in short limbs, fragile bones and cartilage abnormalities. The condition generally results in stillbirth or death during early infancy.
• Asymmetric septal hypertrophy: A disease of the heart muscle characterized by increased thickness of the wall of the heart ventricle which affects the hearts function.
• Atamasco lily poisoning: The atamasco lily is a bulbous plant with long thin leaves and single white or pink flowers. The plant originated in the US. All parts of the plant contain a toxic chemical called lycorine as well as alkaloids. The bulb is the most toxic part of the plant. Eating the bulb can result in death.
• Atelosteogenesis, type 1: A rare genetic disorder characterized by bone formation abnormalities, short stature and early death.
• Athabaskan severe combined immunodeficiency: A severe immunodeficiency disorder found in Navajo and Apache populations.
• Atherosclerosis, premature - deafness - diabetes mellitus - photomyoclonus - nephropathy - degenerative neurologic disease: A rare syndrome characterized mainly by deafness, diabetes, epilepsy, kidney disease and premature hardening of the arteries.
• Ativan overdose: Ativan is a prescription drug mainly used to treat anxiety. Excessive doses of the drug can result in various symptoms and even death in severe cases.
• Atopic asthma: Atopic asthma is one of the most common forms of asthma and is triggered by exposure to an allergen. Upon exposure to the allergen, the airways become constricted and inflamed which affects breathing. The severity of symptoms is variable. This form of asthma is more common in children than adults.
• Atresia of urethra: A rare congenital malformation where the urethra ends blindly which makes it unuseable by the body to eliminate urine. This usually results in death unless surgical intervention provides alternative communication between the bladder and the amniotic sac. In rare cases, there is an abnormal opening between the bladder and the rectum which allow the urine to drain. The inability of the fluid to pass out of the body of the fetus results in a reduced amount of amniotic fluid which in turn affects the development of the lungs.
• Atrial cardiomyopathy with heart block: Atrial heart disease involving a disruption of the electrical signals in the heart and causes heart rhythm problems.
• Atrial fibrillation: A rhythm disturbance of the heart that results in irregular and chaotic ventricular contractions.
• Atrial fibrillation, familial 1: A dominantly inherited condition where abnormal electrical activity in the heart causes it to have a fast and irregular beat. The condition may go unnoticed or may cause stroke or sudden death in some cases.
• Atrial myxoma, familial: An atrial myxoma benign tumor that develops in the wall that separates the two upper chambers of the heart. The familial form of the condition also involves tumors in other parts of the body such as the skin, both heart atria or the heart ventricles.
• Atypical hemolytic uremic syndrome: A rare condition characterized by hemolytic anemia, thrombocytopenia and kidney failure that has no obvious cause.
• Australian Sea Lion poisoning: The Australian Sea Lion is sometimes used as a food source and is found in the South-Southwest waters of Australia. Eating the liver of the Australian Sea Lion can result in a Vitamin A overdose which can cause serious symptoms and even death in extreme cases.
• Austrian syndrome: A condition where alcoholism is associated with heart failure and pneumococcal meningitis.
• Autoimmune Hemolytic Anemia: Autoimmune hemolytic anemia is characterized by an abnormal immune system response which leads to the destruction of red blood cells and hence anemia. The severity of the condition varies depending on the underlying cause e.g. cytomegalovirus, hepatitis, HIV and lupus. The condition may develop gradually or occur suddenly and cause serious symptoms.
• Autonomic Dysreflexia: A complication of spinal cord injury where a particular stimulus can trigger an excessive response from the autonomic nervous system which causes blood pressure to rise - sometimes to dangerous levels. Stimuli that can trigger the response include bladder irritation, bowel irritation (e.g. due to constipation, gas, enema), skin irritation (e.g. due to burns, pressure sores, ingrown toenails), broken bones, tight clothing, labour and temperature extremes. The severity and frequency of the condition is highly variable. The condition occurs in patients with tetraplegia or with loss of sensation above the lower rib cage.
• Autosomal Recessive Polycystic Kidney Disease: Severe form of PKD, a genetic kidney disease.
• Autosomal Recessive Tetra-Amelia: A rare disorder characterized by the absence of all four extremities as well as skeletal, nervous system, craniofacial and other abnormalities. The condition is causes death before or soon after birth.
• Autumn crocus poisoning: The Autumn crocus is a perennial herb which bears purplish-pink flowers. The plant is often used as an ornamental indoor or outdoor plant. The plant contains a chemical called colchicine which can be very poisonous if eaten. The plant is considered to be very toxic if eaten. Boiling the leaves before eating them appears to increase their toxicity. Most cases of poisoning are through accidental ingestion. The plant is sometimes mistaken for wild garlic.
• Azarcon-induced lead poisoning: Azarcon is a lead-containing tetraoxide salt used mainly by Mexican people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• B-cell lymphomas: A group cancers involving the proliferation of lymphocytic B-cells. Examples include small lymphocytic lymphoma, immunoblastic lymphoma and lymphoblastic lymphoma.
• BBB syndrome, X-linked: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: type I is inherited in a X-linked manner and type II is inherited in an autosomal dominant manner. Females with type I tend to have few if any symptoms - often the only symptom is wide-set eyes.
• Ba Bow Sen-induced lead poisoning: Ba Bow Sen is a folk remedy used mainly by Chinese people to treat childhood hyperactivity and to alleviate nightmares. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Bacterial pericarditis: Inflammation and swelling of the pericardium (fibrous sac surrounding the heart) due to a bacterial infection. It can occur as a complication of a bacterial infection in some other part of the body. It is most often a complication of a respiratory infection but skin and oral infections may also be a cause. Bacterial pericarditis may also occur after heart surgery. It occurs predominantly in males aged 20 to 50 years. The condition may be misdiagnosed as a heart attack and vice versa.
• Bacterial toxic-shock syndrome: A very rare, potentially fatal infection caused by toxins produced by bacteria, especially bacteria such as Staphylococcus aureus or Streptococcus pyogenes. The condition is often associated with tampon use but can originate from other sources.
• Bali goli-induced lead poisoning: Bali goli (flat black bean) is a folk remedy used mainly by Indian and Asian people to treat intestinal problems. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Balo disease: A rare neurological disorder where the protective sheath around brain nerve fibres are progressively destroyed. Symptoms are determined by the size and location of the affected brain area.
• Baltic myoclonic epilepsy: A rare inherited type of progressive myoclonus epilepsy which tends to cause symptoms during childhood. The involuntary muscle movements tend to occur more frequently and become more severe with increasing age. Symptoms may occur following various stimuli such as light, stress or exercise.
• Bard-Pic syndrome: A complication of advanced pancreatic cancer marked by jaundice and enlarged gallbladder.
• Bare lymphocyte syndrome: An inherited immunodeficiency disorder characterized by T- and B-cell dysfunction (these cells are essential for helping fight infection). Lack of treatment can result in infant death from infection.
• Batten Disease: Rare childhood genetic degenerative nerve system disease.
• Beemer-Ertbruggen syndrome: A rare lethal syndrome characterized primarily by hydrocephalus, heart malformations, and increased bone density. Only a couple of cases have been reported.
• Bell mania: A rare life-threatening neuropsychiatric disorder involving delusions, hyperactivity and periods of fever. Death can occur within days or months without treatment.
• Berardinelli-Seip congenital lipodystrophy, type 2: A rare genetic disorder characterized by early-onset diabetes mellitus, loss of body fat, serious insulin resistance, high blood triglycerides and fatty liver. Type 2 is distinguished from type 2 by the origin of the genetic defect. Type 2 is caused by a defect on the BSCL2 gene on chromosome 11q13. Type 2 seems to be more severe with some cases resulting in premature death which can occur as early as the first year of life. Type 2 also involves mental retardation which is not seen in type 1.
• Bernheim's syndrome: Reduced size of right heart ventricle due to enlargement of the left ventricle which encroaches on the space in the right ventricle. Blood flow from the right atrium to the right ventricle is obstructed.
• Berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification: A very rare syndrome characterized primarily by brain aneurysms, liver cirrhosis, pulmonary emphysema and calcification of the brain (cerebrum).
• Bickerstaff's brainstem encephalitis: A rare condition where inflammation of the brainstem results in various symptoms such as ataxia and ophthalmoplegia. The onset of symptoms is usually acute.
• Bickerstaff's brainstem encephalitis (BBE): A rare condition where inflammation of the brainstem results in various symptoms such as ataxia and ophthalmoplegia. The onset of symptoms is usually acute.
• Bidirectional tachycardia: A rare form of abnormal heart rhythm. Causes includes digitalis toxicity, certain heart malformations and hyperkalemic periodic paralysis.
• Bilateral renal agenesis dominant type: A rare birth defect where both kidneys are absent. The disorder results in death within days of birth.
• Bile duct cancer, extrahepatic: A rare cancer that develops in the part of the common bile duct that is outside the liver. The common bile duct channels bile from the gall bladder (which stores bile) and the liver (which makes bile) to the small intestine to assist digestion.
• Biliary atresia, intrahepatic, non syndromic form: Congenital obstruction of the passages in the liver that carry bile. The nonsyndromic form is not associated with any other abnormalities.
• Biliary atresia, intrahepatic, syndromic form: Congenital obstruction of the passages in the liver that carry bile. The syndromic form is associated with other congenital abnormalities such as heart and visceral defects.
• Biliary cirrhosis: Biliary cirrhosis is a condition where the bile ducts are unable to transport bile effectively due to blockage, inflammation, scarring or some other damage to the bile ducts. The condition may result from such things as congenital defect of the bile ducts (e.g. biliary atresia), cystic fibrosis, gallstones or a variety of other secondary conditions. The cause of primary biliary cirrhosis is not fully understood.
• Biliary tract cancer: Cancer that develops in the gallbladder or bile ducts.
• Bing-Neel syndrome: A rare disorder involving infiltration of the central nervous system by abnormal leukemia-like cells (lymphoplasmocytoid cells) that occur in Waldenström's macroglobulinemia. The abnormality increases blood viscosity which impairs its circulation through small brain and eye blood vessels.
• Bint Al Zahab-induced lead poisoning: Bint Al Zahab is a folk remedy used by various ethnic groups (e.g. Indians, Saudi Arabians) to treat infant colic and to facilitate the passage of meconium in newborns. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Bird cherry seed poisoning: Wild cherry seeds contain a chemical called amygdalin which breaks down into cyanide in the human body. The toxic chemicals are not released if the seed remains intact and therefore poisoning usually occurs if the seeds are crushed and eaten. Accidental ingestion is very unusual.
• Bird flu (avian influenza): Bird flu refers to influenza A invection. Influenza A is a viral respiratory infection that can usually occurs in birds (especially poultry) but can be transmitted to humans and cause serious illness. The virus is contagious and can cause severe illness especially in patients who are very young or old or have some other medical condition as well. The severity of symptoms can vary but usually involves respiratory and constitutional (e.g. headache, aching muscles) symptoms. The influenza virus can mutate and produce different strains though the symptoms are the same. This frequent mutation means that people need regular vaccinations to ensure they are protected against new strains as they arise.
• Bitter almond seed poisoning: Bitter almond seeds contain a chemical called amygdalin which breaks down into cyanide in the human body. Accidental ingestion is very unusual. Bitter almond plants grow mainly in Northern America. Various processes can be used to leach the toxic chemical out of the bitter almonds.
• Black henbane poisoning: Black henbane is a herb which has hairy stems and bears flowers and fruit. All parts of the plant contain tropane alkaloids which is toxic enough to cause death if eaten. Black henbane is often used for medicinal purposes to treat a variety of health conditions.
• Black jetbead poisoning: The Black jetbead is a deciduous shrub which bears single white flowers and small groups of shiny black fruit. The fruit contains amygdalin which is very toxic and can cause severe poisoning or even death if eaten.
• Black locust poisoning: The black locust is a large deciduous tree which has long clusters of scented flowers and flat fruit pods. The young leaves, seeds and inner bark contain various chemicals (robin, robinine and robitin) which can be toxic if large quantities are eaten. The flowers are considered edible if handled correctly.
• Black nightshade poisoning: The Black Nightshade is a herb which bears small white or purple flowers and dull black berries. The plant originated in South America. The berries contain solanine alkaloid which can be toxic if eaten in large quantities. The leaves and unripe berries are considered toxic whereas the ripe fruit is possibly edible.
• Black widow spider envenomation: The black widow spider bite is toxic to the nerves and can cause serious symptoms. The black widow spider is most commonly found in North America.
• Bland-Garland-White syndrome: A rare birth malformation where the left coronary artery comes out of the pulmonary artery instead of the aorta. Usually, infants are usually healthy for a few months after which they start having symptoms of heart problems. Occasionally, patients may be asymptomatic even into adulthood but usually death occurs during infancy.
• Bland-White -Garland syndrome: A heart disorder where the left coronary artery comes out of the pulmonary artery.
• Blast crisis: The final phase of chronic myeloid leukemia which has a high mortality rate. Myeloid leukemia is a form of cancer where the bone marrow makes too many myeloid cells (granulocytes and their precursors) in the bone marrow which accumulates in the blood and eventually invades various parts of the body. The three phases of the condition are the chronic phase, aggressive phase and finally the blast crisis. A blast crisis is occurs when over 30% of the cells in the blood or bone marrow are immature blood cells (blast cells). Patients in the final stage of leukemia are more prone to relapses following treatment.
• Blastoma: A type of tumor that originates from precursor cells or blasts (immature or embryonic tissue). The symptoms can vary greatly and are determined by the part of the body that is affected. Blastomas can occur in parts of the body such as the brain, liver, kidneys, nervous system, bones and the retina.
• Bleeding symptoms: Any type of bleeding symptoms.
• Blepharophimosis - nasal groove - growth delay: A very rare syndrome characterized mainly by eyelid abnormalities, retarded growth and a nasal groove.
• Blepharophimosis - nasal groove - growth retardation: A very rare syndrome characterized mainly by eyelid abnormalities, retarded growth and a nasal groove.
• Blepharophimosis, large cylindrical nose and severe intrauterine growth retardation: A rare syndrome characterized by eye and nose anomalies as well as severely retarded fetal growth.
• Blood coagulation disorders, inherited: Inherited blood disorders where the ability to form clots is dysfunctional. The blood needs to be able to clot to prevent excessive bleeding in situations such as when the body suffers some sort of injury. With blood coagulation disorders, the blood's ability to clot may be impaired, resulting in excessive bleeding, or the blood may form clots too readily and result in thrombosis.
• Bloodroot poisoning: The Bloodroot is a flowering herb that bears fruit and whose stem contains red juices. The plant tends to grow in mountainous areas. The thickened roots (rhizomes) of the plant contain isoquinoline alkaloids which are very toxic and can cause death if eaten in sufficient quantities.
• Blue-ringed octopus poisoning: The blue-ringed octopus is found in shallow Australian ocean water and can deliver venomous, potentially fatal bite. The poison is present in the saliva of the octopus. The venom affects the neuromuscular system.
• Body packer syndrome: Consuming packages of drugs for the purpose of concealing them for transportation.
• Bokhoor-induced lead poisoning: Bokhoor is a traditional used mainly by Saudi Arabian people to calm infants - it involves burning wood and lead sulphide and inhaling the fumes that are produced. This practice has the potential to cause lead poisoning due to the relatively high exposure to lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Bolivian hemorrhagic fever: An infectious disease that occurs in Bolivia and is caused by the Machupo virus. Transmission can occur through contact with infected rodent (Calomys callosus) droppings. The incubation period lasts from one to two weeks.
• Bone cement implantation syndrome: A complication that can occur after using bone cement during implantation of an internal prosthesis. Circulation may be affected and a blockage in the pulmonary artery may develop.
• Bone dysplasia with medullary fibrosarcoma: A rare inherited bone disorder characterized by aggressive bone tumors and defective bone development. The tumors metastasized readily.
• Bone dysplasia, lethal, Holmgren type: A rare lethal bone malformation syndrome.
• Bone symptoms: Symptoms affecting the body's bones
• Bonefish poisoning (clupeotoxin): Some bonefish contain toxins (Clupeotoxin) which can be poisonous to humans if eaten. Heat does not destroy the toxin and there is still uncertainty as to the origin of the toxin. The toxin appears to be present in higher concentrations in summer and is believed to be possible linked to the consumption of toxic food in its food web. The size and age of the bonefish does not appear to be related to the toxicity. The bonefish are found in coastal waters off Africa and the Caribbean, Indian and Pacific Oceans.
• Boomerang dysplasia: A rare lethal disorder characterized by bone abnormalities (lack of bone ossification and missing bones) and a characteristic face.
• Bottlebrush buckeye poisoning: The Bottlebrush buckeye is a deciduous shrub which bears clusters of white or pink flowers and smooth, leathery fruit containing shiny seeds. The plant originated in southern USA. The plant contains various toxic chemicals (glycoside esculin, saponin aescin) which can cause potentially fatal toxicity if sufficient quantities of the seeds or leaves are consumed.
• Botulism food poisoning: Extremely dangerous food poisoning requiring medical attention, but not always recognized because of its non-abdominal symptoms.
• Boutonneuse fever: An infectious disease that is caused by Rickettsia conorii which is transmitted by the brown dog tick (Rhipicephalus sanguineus). The disease occurs predominantly in Mediterranean areas such as India and Africa. The onset of symptoms is usually sudden and the incubation period is usually between 6 and 10 days.
• Box Jellyfish poisoning: A sting from the Box jellyfish contains a chemical which is toxic to the nerves, heart and skin. This jellyfish is mainly found in the waters of Northern Queensland in Australia. The tentacles should not be removed from the patient as it can cause further injection of poison.
• Brachymesomelia-renal syndrome: A rare syndrome characterized by kidney abnormalities and forearm and lower leg deformity. The condition describes a single reported case.
• Brain abscess: abscess in the brain may involve any of the lobes of the brain
• Brain malformation - congenital heart disease - postaxial polydactyly: A very rare syndrome characterized mainly by a brain defect, congenital heart disease and extra fingers.
• Brain symptoms: Symptoms affecting the brain
• Brain tumor, adult: A growth or tumor that develops in the tissues of the brain in adults. The tumor can be benign or malignant.
• Breathing difficulties: Various types of breathing difficulty (dyspnea).
• Brinton disease: Thickening and hardening of the stomach wall usually associated with diffuse stomach cancer or damage due to the consumption of caustic soda.
• Bristowe's syndrome: Symptoms caused by a brain tumor that develops in the corpus callosum which connects the two brain hemispheres.
• Brittle bone syndrome lethal type: A rare form of brittle bone disease caused by abnormal collagen production which results in weak bones which break easily. The condition can result in death, especially during the process of birth which can result in multiple severe fractures.
• Broad bean poisoning: The broad bean is a vine which produces pea-like flowers and long, seed-filled pods. The seeds can be very toxic and can result in death if eaten. This toxic reaction only occurs to certain susceptible people who are unable to process certain chemicals in the plant. The resulting condition is called favism and is most common in people of Mediterranean descent.
• Bronchiolitis: A condition which is characterized by inflammation of the bronchioles
• Bronchiolitis Obliterans - Ammonia inhalation: A lung disease caused by inhalation of Ammonia. The exposure can cause scarring of the lungs which can lead to obstruction of the small airways and ultimately impaired lung function. Chronic exposure can lead to gradual worsening of symptoms over a period of time. Acute exposure can result in lung damage that may be asymptomatic for a short period of time but can then lead to rapid death due to severe obstructive breathing problems. Severity of symptoms and outcome depend on degree of exposure.
• Bronchiolitis Obliterans - Chlorine inhalation: A lung disease caused by inhalation of Chlorine. The exposure can cause scarring of the lungs which can lead to obstruction of the small airways and ultimately impaired lung function. Chronic exposure can lead to gradual worsening of symptoms over a period of time. Acute exposure can result in lung damage that may be asymptomatic for a short period of time but can then lead to rapid death due to severe obstructive breathing problems. Severity of symptoms and outcome depend on degree of exposure.
• Bronchiolitis Obliterans - Diacetyl inhalation: A lung disease caused by inhalation of Diacetyl. The exposure can cause scarring of the lungs which can lead to obstruction of the small airways and ultimately impaired lung function. Chronic exposure can lead to gradual worsening of symptoms over a period of time. Acute exposure can result in lung damage that may be asymptomatic for a short period of time but can then lead to rapid death due to severe obstructive breathing problems. Severity of symptoms and outcome depend on degree of exposure.
• Bronchiolitis Obliterans - Hydrogen bromide inhalation: A lung disease caused by inhalation of Hydrogen bromide. The exposure can cause scarring of the lungs which can lead to obstruction of the small airways and ultimately impaired lung function. Chronic exposure can lead to gradual worsening of symptoms over a period of time. Acute exposure can result in lung damage that may be asymptomatic for a short period of time but can then lead to rapid death due to severe obstructive breathing problems. Severity of symptoms and outcome depend on degree of exposure.
• Bronchiolitis Obliterans - Hydrogen chloride inhalation: A lung disease caused by inhalation of Hydrogen chloride. The exposure can cause scarring of the lungs which can lead to obstruction of the small airways and ultimately impaired lung function. Chronic exposure can lead to gradual worsening of symptoms over a period of time. Acute exposure can result in lung damage that may be asymptomatic for a short period of time but can then lead to rapid death due to severe obstructive breathing problems. Severity of symptoms and outcome depend on degree of exposure.
• Bronchiolitis Obliterans - Hydrogen fluoride inhalation: A lung disease caused by inhalation of Hydrogen fluoride. The exposure can cause scarring of the lungs which can lead to obstruction of the small airways and ultimately impaired lung function. Chronic exposure can lead to gradual worsening of symptoms over a period of time. Acute exposure can result in lung damage that may be asymptomatic for a short period of time but can then lead to rapid death due to severe obstructive breathing problems. Severity of symptoms and outcome depend on degree of exposure.
• Bronchiolitis Obliterans - Hydrogen sulfide inhalation: A lung disease caused by inhalation of Hydrogen sulfide. The exposure can cause scarring of the lungs which can lead to obstruction of the small airways and ultimately impaired lung function. Chronic exposure can lead to gradual worsening of symptoms over a period of time. Acute exposure can result in lung damage that may be asymptomatic for a short period of time but can then lead to rapid death due to severe obstructive breathing problems. Severity of symptoms and outcome depend on degree of exposure.
• Bronchiolitis Obliterans - Methyl isocyanate inhalation: A lung disease caused by inhalation of Methyl isocyanate. The exposure can cause scarring of the lungs which can lead to obstruction of the small airways and ultimately impaired lung function. Chronic exposure can lead to gradual worsening of symptoms over a period of time. Acute exposure can result in lung damage that may be asymptomatic for a short period of time but can then lead to rapid death due to severe obstructive breathing problems. Severity of symptoms and outcome depend on degree of exposure.
• Bronchiolitis Obliterans - Nitrogen Oxide inhalation: A lung disease caused by inhalation of Nitrogen oxides. The exposure can cause scarring of the lungs which can lead to obstruction of the small airways and ultimately impaired lung function. Chronic exposure can lead to gradual worsening of symptoms over a period of time. Acute exposure can result in lung damage that may be asymptomatic for a short period of time but can then lead to rapid death due to severe obstructive breathing problems. Severity of symptoms and outcome depend on degree of exposure.
• Bronchiolitis Obliterans - Ozone inhalation: A lung disease caused by inhalation of v. The exposure can cause scarring of the lungs which can lead to obstruction of the small airways and ultimately impaired lung function. Chronic exposure can lead to gradual worsening of symptoms over a period of time. Acute exposure can result in lung damage that may be asymptomatic for a short period of time but can then lead to rapid death due to severe obstructive breathing problems. Severity of symptoms and outcome depend on degree of exposure.
• Bronchiolitis Obliterans - Phosgene inhalation: A lung disease caused by inhalation of Nitrogen oxides. The exposure can cause scarring of the lungs which can lead to obstruction of the small airways and ultimately impaired lung function. Chronic exposure can lead to gradual worsening of symptoms over a period of time. Acute exposure can result in lung damage that may be asymptomatic for a short period of time but can then lead to rapid death due to severe obstructive breathing problems. Severity of symptoms and outcome depend on degree of exposure.
• Bronchiolitis Obliterans - Polyamide-amine dyes inhalation: A lung disease caused by inhalation of Polyamide-amine dyes. The exposure can cause scarring of the lungs which can lead to obstruction of the small airways and ultimately impaired lung function. Chronic exposure can lead to gradual worsening of symptoms over a period of time. Acute exposure can result in lung damage that may be asymptomatic for a short period of time but can then lead to rapid death due to severe obstructive breathing problems. Severity of symptoms and outcome depend on degree of exposure.
• Bronchiolitis Obliterans - Sulphur dioxide inhalation: A lung disease caused by inhalation of Sulphur dioxide. The exposure can cause scarring of the lungs which can lead to obstruction of the small airways and ultimately impaired lung function. Chronic exposure can lead to gradual worsening of symptoms over a period of time. Acute exposure can result in lung damage that may be asymptomatic for a short period of time but can then lead to rapid death due to severe obstructive breathing problems. Severity of symptoms and outcome depend on degree of exposure.
• Bronchiolitis Obliterans - Thionyl chloride inhalation: A lung disease caused by inhalation of Thionyl chloride. The exposure can cause scarring of the lungs which can lead to obstruction of the small airways and ultimately impaired lung function. Chronic exposure can lead to gradual worsening of symptoms over a period of time. Acute exposure can result in lung damage that may be asymptomatic for a short period of time but can then lead to rapid death due to severe obstructive breathing problems. Severity of symptoms and outcome depend on degree of exposure.
• Bronchiolitis obliterans with obstructive pulmonary disease: A rare condition involving the inflammation and thickening of the internal lung structures (bronchioles) which affects breathing. It can be triggered by certain infections, drug reactions or for no obvious reason. The condition often progresses to cause serious respiratory problems or even death though the rate of disease progression is variable.
• Bronchopulmonary dysplasia: A condition which is characterized by dysplasia of the brochopulmonary vessels
• Brown Recluse spider poisoning: The Brown Recluse spider is poisonous and is found mainly in southern and central areas of the US.
• Brown snake poisoning: The Brown snake is a poisonous Australian snake. They are considered one of the most venomous snakes in the world and their bite can result in death without prompt medical attention. The snake venom contains toxins which affect the blood and nerve systems. Children tend to suffer more severe symptoms due to their smaller body size.
• Brown-Symmers disease: A rare form of brain inflammation that occurs in children and can quickly lead to death. Symptoms usually start suddenly.
• Bruch's disease: An infectious disease that is caused by Rickettsia conorii which is transmitted by the brown dog tick (Rhipicephalus sanguineus). The disease occurs predominantly in Mediterranean areas such as India and Africa. The onset of symptoms is usually sudden and the incubation period is usually between 6 and 10 days.
• Brugada Syndrome: A rare genetic disorder characterized by heart rhythm abnormalities which can result in sudden death if untreated. The condition may be inherited in some cases. The mean age of sudden death is 40 years of age.
• Brugada syndrome 1: A rare genetic disorder characterized by heart rhythm abnormalities which can result in sudden death if untreated. Type 1 is caused by a mutation in the SCN5A gene on chromosome 3p21. Symptoms most often occur during the night and the condition is most prevalent in Japan and Southeast Asia.
• Brugada syndrome 2: A rare genetic disorder characterized by heart rhythm abnormalities which can result in sudden death if untreated. Type 2 is caused by a mutation in the GPD1L gene on chromosome 3p22.3. Symptoms most often occur during the night and the condition is most prevalent in Japan and Southeast Asia.
• Brugada syndrome 3: A rare genetic disorder characterized by heart rhythm abnormalities which can result in sudden death if untreated. Type 3 is caused by a mutation in the CACNA1C gene on chromosome 12p13.3. Symptoms most often occur during the night and the condition is most prevalent in Japan and Southeast Asia.
• Brugada syndrome 4: A rare genetic disorder characterized by heart rhythm abnormalities which can result in sudden death if untreated. Type 14 is caused by a mutation in the CACNB2 gene on chromosome 10p12. Symptoms most often occur during the night and the condition is most prevalent in Japan and Southeast Asia.
• Budd chiari syndrome: A disorder where the main vein leaving the liver becomes blocked leading to symptoms such as liver enlargement and fluid buildup in the abdomen. Also called Chiari's syndrome or Rokitansky's disease.
• Bufotenine poisoning: The skin glands of certain toads (Cane toad and Colorado river toad) contain a poison called bufotoxin.
• Bulimia nervosa: Eating disorder with binging (overeating) and purging (vomiting).
• Bullous dystrophy, macular type: A rare condition characterized by loss of scalp hair, increased skin pigmentation, small head, mental retardation, short stature and blisters. The blisters do not form necessarily on skin that has suffered trauma but occurs spontaneously.
• Burnett's milk drinker's syndrome: Burnett's milk drinker's syndrome is a condition where the body is too alkaline and the blood contains too much calcium which results in impaired kidney function. It can be caused by drinking large quantities of milk or using too many alkaline antacid remedies. High vitamin D intake can make the condition worse. The people most at risk of this condition tend to be older people (especially women) who are taking calcium supplements as well as calcium carbonate containing remedies to treat dyspepsia.
• Burnett's syndrome: Burnett's syndrome is a condition where the body is too alkaline and the blood contains too much calcium which results in impaired kidney function. It can be caused by drinking large quantities of milk or using too many alkaline antacid remedies. High vitamin D intake can make the condition worse. The people most at risk of this condition tend to be older people (especially women) who are taking calcium supplements as well as calcium carbonate containing remedies to treat dyspepsia.
• Burns: Injury from burns and scalds.
• Bushmaster poisoning: The Bushmaster is a poisonous snake found in America.
• Bywaters' syndrome: A trauma or accident involving the crushing of soft tissues and associated symptoms. Severe cases can result in death.
• C1esterase deficiency: C1esterase deficiency is a condition characterized by swelling under the skin or mucosal tissue - the skin, respiratory tract or gastrointestinal tract may be affected. The condition may be inherited or acquired. Symptoms tend to develop over a few days and then abate after two to five days. Swelling attacks may occur fairly regularly e.g. weekly or sporadically e.g. once or twice a year.
• CDG syndrome (generic term): Congenital disorders of glycosylation is a group of very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. The main symptom in all the disorders is psychomotor retardation but other variable symptoms also occur depending on the subtype of the disorder.
• CDG syndrome type 3: Congenital disorders of glycosylation is a group of very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 3 has variable symptoms.
• CDG syndrome type I: A rare genetic disorder where the body is unable to synthesize glycoproteins which results in multisystem problems.
• CML-Like Syndrome, Familial: A very rare condition characterized by symptom similar to myelocytic leukemia that develop during infancy. The condition can result in death during the first years of life.
• CMV antenatal infection: A rare condition where a fetus becomes infected with the cytomegalovirus through the mother.
• COACH syndrome: A very rare syndrome characterized by ataxia, gaps or holes in various eye structures, mental retardation, liver fibrosis and brain abnormalities.
• COPD: Severe obstruction of bronchial air flow typically from bronchitis and/or emphysema.
• Calcific aortic disease with immunologic abnormalities, familial: A rare familial condition characterized by the abnormal calcification of the aorta and aortic valve. The calcification can narrow the aortic valve opening and hence affect blood flow. The condition also includes immunological abnormalities
• California buckeye poisoning: The California buckeye is a deciduous shrub which bears clusters of white or pink flowers and smooth, leathery fruit containing shiny seeds. The plant originated in California. The plant contains various toxic chemicals (glycoside esculin, saponin aescin) which can cause potentially fatal toxicity if sufficient quantities of the seeds or leaves are consumed.
• California encephalitis: An uncommon mosquito born virus (California encephalitis virus) which can cause brain inflammation in humans. The severity of symptoms is variable. The incubation period can last from a few days to a week. Infants and children tend to be more severely affected than adults who sometimes have no obvious symptoms.
• Calla lily poisoning: A bulb plant which bears large colored or white flower-like structure on long leafless stems. It is often grown in gardens or used in flower arrangements. The plant contains chemicals including calcium oxalate crystals which are highly toxic if eaten. Death can result if sufficient quantities are eaten.
• Campomelia Cumming type: A rare syndrome characterized by limb and multiple abdominal organ abnormalities. The disorder results in death before birth or soon after.
• Campomelic dwarfism: A rare genetic disorder characterized by bowed tibia, underdeveloped shoulder blades and a flat face.
• Campomelic dysplasia: A rare genetic disorder characterized by bowed tibia, underdeveloped shoulder blades and a flat face.
• Campylobacter fetus infection: Campylobacter fetus is a food borne bacterial infection which may vary in severity from mild to severe. The bacteria are opportunistic and mainly affect debilitated patients but can also occur in healthy patients. Abortion due to blood infection in the fetus can occur in pregnant women who become infected. The infection is less likely to cause gastrointestinal symptoms such as diarrhea than other Campylobacter infections but is prone to causing infection in other parts of the body such as the appendix, abdominal cavity, central nervous system (meningitis), gallbladder, urinary tract and blood stream. Cattle and sheep are the main source of this bacteria.
• Campylobacter hylointestinalis infection: Campylobacter hyloinstesinalis is a food borne bacterial infection which may cause mild to severe gastroenteritis. Cattle, pigs, hamsters and deer are the main source of this bacteria.
• Campylobacter jejuni infection: Campylobacter jejuni infection is a common food borne bacterial infection which may vary in severity from mild to severe. Death can occur in severe cases but tends to occur in patients with other existing illnesses such as HIV, cancer or liver disease. The infection can in rare cause infection in other parts of the body such as the appendix, abdominal cavity, central nervous system (meningitis), gallbladder, urinary tract and blood stream. Undercooked chicken is the main source of infection.
• Campylobacter jejuni subspecies doylei infection: A bacterial infection that involves bacteria from the Campylobacter family. It tends to cause gastrointestinal symptoms.
• Canada moonseed poisoning: The Canada moonseed is a woody deciduous vine which bears clusters of bluish or blackish fruit. The fruit is distinguished by the presence of crescent-shaped seeds. The fruit contains dauricine which is very toxic and can result in death if sufficient quantities are consumed.
• Capillaria philippiensis infection: A fish borne parasite that can infect humans. Transmission most often occurs through ingestion of contaminated fish. Severity of symptoms tend to increase as the number of worms multiply in the intestines. Death can occur if the condition is left untreated.
• Capillary leak syndrome with monoclonal gammopathy: A rare condition characterized by leaky blood vessels and an increased level of certain blood proteins (monoclonal gammopathy). Monoclonal gammopathy itself does not cause any symptoms unless it develops into plasma cell leukemia. The condition may vary from mild to severe enough to cause death.
• Capnocytophaga: A bacterial infection caused by Capnocytophaga canimorsus which is often found in normal healthy cats and dogs. The infections tends to occur mainly in immunocompromised patients, alcoholics or patients who have chronic respiratory disease or have had their spleen removed. The eyes are particularly sensitive to this infection. The incubation period can be as long as eight days.
• Carbamoyl-phosphate synthase 1 deficiency: A very rare inherited urea cycle disorder where the lack of the enzyme carbamoyl phosphate synthetase prevents ammonia from being turned into urea and being excreted in the urine. Excess ammonia builds up in the body which can cause serious complications or even death if left untreated.
• Carbon disulfide-induced cardiovascular disease: Chronic exposure to certain chemicals can cause cardiovascular disease. For example, exposure to Carbon disulfide can lead to heart disease and carries a risk of premature death as a result. Chronic exposure to these sort of chemicals is most likely to occur in a work environment. Carbon disulfide is used mainly in viscose rayon manufacturing but is also used as a solvent and in other process. Exposure usually occurs through inhalation of vapours but skin absorption can also occur. Reported cases haf cardiovascular disease has occurred among workers exposed to carbon disulfide concentrations of 20-60 ppm.
• Carcinoma of the vocal tract: Cancer of the vocal cords in the larynx.
• Carcinoma, squamous cell of head and neck: A type of cancer that occurs in the mucosal lining of parts of the head and neck e.g. esophagus, sinuses, nasal cavity, pharynx, mouth and lips. Symptoms will vary depending on the exact location of the cancer.
• Cardiac diverticulum: A rare congenital heart malformation involving the outpouching (diverticulum) of a ventricle which can affect heart function to varying degrees depending on the size and location of the defect.
• Cardiac hydatid cysts with intracavitary expansion: A parasitic infection that occurs in the heart. Hydatid cyst is the larval stage of a parasite called echinococcus granulosus. Symptoms will depend on the exact location of the cyst. Usually the liver and lungs are involved.
• Cardiac malformation: Any malformation or structural defect of the heart or it's structures. Some examples include atrioventricular septal defect, conotruncal malformations, transposition of great vessels and heart valve dysplasia. The symptoms vary in nature and severity depending on the type of malformation.
• Cardioencephalomyopathy fatal infantile due to cytochrome c oxidase deficiency: A very rare inherited metabolic disorder where the body doesn't have enough of an enzyme called cytochrome C oxidase (COX) which is needed in the process of energy production by body cells. The fatal infant type generally affects the hear, brain and kidneys as well as the muscles.
• Cardiomyopathy - hearing loss, type t RNA lysine gene mutation: A rare inherited disorder characterized by heart muscle disease and deafness. The deafness is inherited from the mother and is caused by a genetic defect. Patients may be asymptomatic for a number of years. The rate of progression of the disorder is variable with some patients being asymptomatic until adulthood.
• Cardiomyopathy - hypotonia - lactic acidosis: A rare syndrome characterized by heart muscle disease, reduced muscle tone and lactic acidosis from birth.
• Cardiomyopathy dilated 10: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the heart's ability to function normally. The disorder is caused by the degeneration of the heart's conduction system. Type 10 is caused by a defect in the ABC9 gene on chromosome 12p12.1.
• Cardiomyopathy dilated 1B: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Type 1B is caused by a defect on chromosome 9q13.
• Cardiomyopathy dilated 1C: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Type 1C is caused by a defect in the LDB3 gene on chromosome 10q21-q23.
• Cardiomyopathy dilated 1D: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Type 1D is caused by a defect in the cardiac troponin gene on chromosome 1q32.
• Cardiomyopathy dilated 1G: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Type 1G is caused by a defect in the titin gene on chromosome 2q24.3.
• Cardiomyopathy dilated 1H: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Type 1H is caused by a defect on chromosome 2q14-q22.
• Cardiomyopathy dilated 1I: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Type 1I is caused by a defect in the desmin gene on chromosome 2q35.
• Cardiomyopathy dilated 1J: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Hearing impairment also becomes apparent by the end of the second decade. Type 1J is caused by a defect in the LDB3 gene on chromosome 6q23.
• Cardiomyopathy dilated 1K: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Type 1K is caused by a defect on chromosome 6q12-q16.
• Cardiomyopathy dilated 1L: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Type 1L is caused by a defect in the delta-sarcoglycan gene on chromosome 5q33.
• Cardiomyopathy dilated 1M: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Type 1M is caused by a defect in the CSRP3 gene on chromosome 11p15.1.
• Cardiomyopathy dilated 1N: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Type 1N is caused by a defect in the telethonin gene on chromosome 17q12.
• Cardiomyopathy dilated 1P: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Type 1P is caused by a defect in the phospholamban gene on chromosome 6q22.1.
• Cardiomyopathy dilated 1Q: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Type 1Q is caused by a defect on chromosome 7q22.3-q31.1.
• Cardiomyopathy dilated 1R: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Type 1R is caused by a defect in the ACTC gene on chromosome 15q14.
• Cardiomyopathy dilated 1S: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Type 1S is caused by a defect in the heavy chain myosin 7 gene on chromosome 14q12.
• Cardiomyopathy dilated 1T: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Type 1T is caused by a defect in the TMPO gene on chromosome 12q22.
• Cardiomyopathy dilated 1U: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Type 1U is caused by a defect in the PSEN1 gene on chromosome 14q24.3.
• Cardiomyopathy dilated 1W: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Type 1W is caused by a defect in the metavinculin gene on chromosome 10q22.1-q23.
• Cardiomyopathy dilated 1Y: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the heart's conduction system. Type 1Y is caused by a genetic defect on chromosome 15q25.1.
• Cardiomyopathy dilated 1Z: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the heart's conduction system. Type 1Z is caused by a genetic defect on chromosome 3p21.2-p14.3.
• Cardiomyopathy dilated with conduction defect: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system.
• Cardiomyopathy dilated with conduction defect type 1: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Type 1 is caused by a defect in the lamin A/C gene on chromosome 1q21.
• Cardiomyopathy dilated with conduction defect type 2: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the hearts conduction system. Type 2 is caused by a defect in the cardiac sodium channel gene on chromosome 3p21.
• Cardiomyopathy, X-linked, fatal infantile: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The condition occurs during infancy and results in death.
• Cardiomyopathy, familial dilated: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally.
• Cardiomyopathy, fatal fetal, due to myocardial calcification: A rare syndrome characterized by heart muscle disease caused by calcium deposits in the heart muscle. The disorder causes fetal death.
• Carnitine transporter deficiency: An inherited deficiency of carnitine caused by the impaired ability of the carnitine transporter protein to carry the carnitine to where it is needed. Instead the carnitine is excreted through the urine. Fasting or illness can trigger a severe attack.
• Carolina Cherry Laurel poisoning: The Carolina cherry laurel is an evergreen tree which bears small white flowers and small green fruit which turns black when ripe. Most parts of the plant contain cyanogenic glycoside and amygdalin which can cause symptoms if ingested. The plant is considered highly toxic and eating sufficient quantities can lead to death.
• Carotid Paraganglioma: A rare, usually benign tumor found in the carotid artery in the neck. The tumor develops from glomus cells which are located along blood vessels involved in automatic body activities such as regulation of blood pressure and blood flow.
• Cartilaginous neoplasms: Tumors made up of cartilage tissue. The tumors may be benign or malignant and the symptoms will depend on the location and size of the tumors. The tumors can form on parts of the body such as the arm and leg bones or even in the pharynx. The tumors may cause no symptoms in some cases and are only discovered incidentally.
• Cataract and cardiomyopathy: A rare syndrome characterized by the association of congenital cataracts, heart muscle disease, lactic acidosis and skeletal muscle disease. The disorder involves the abnormal storage of lipids and glycogen in the skeletal and heart muscles. The cataracts progress rapidly and require surgery. The severity of the disorder ranges from stillbirth to survival into the fourth decade.
• Catastrophic Antiphospholipid Syndrome: A very rare disorder where the blood clotting system becomes dysfunctional and clots too easily due to the abnormal presence of antphospholipid antibodies. It results in blood flow blockages to various body organs. It is possible that the condition has autoimmune origins. The disorder is often triggered by infections, certain drugs (e.g. anticoagulants), minor surgery and hysterectomy.
• Caterpillar-induced bleeding syndrome: Caterpillars from the Lonomia genus have spines along their body which can penetrate human skin and cause blood coagulation problems. The severity of the symptoms vary depending on the degree of envenomation but serious cases can result in death.
• Caterpillar-induced bleeding syndrome - Lonomia achelous: Lonomia achelous caterpillars are native to Northern Brazil and Venezuela. They have spines along their body which can penetrate human skin and cause blood coagulation problems. The severity of the symptoms vary depending on the degree of envenomation but serious cases can result in death.
• Caterpillar-induced bleeding syndrome - Lonomia obliqua: Lonomia obliqua caterpillars are native to Southern Brazil and have spines along their body which can penetrate human skin and cause blood coagulation problems. The severity of the symptoms vary depending on the degree of envenomation but serious cases can result in death.
• Cebagin-induced lead poisoning: Cebagin is a folk remedy used mainly by Middle Eastern people to treat teething. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Ceftazidime - Teratogenic Agent: There is evidence to indicate that exposure to Ceftazidime (an antibiotic) during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
• Central nervous system lymphoma, primary: A type of lymphoma that occurs in the central nervous system (brain and spinal cord). A lymphoma consists of cancerous lymphocytes which are a type of white blood cell. Symptoms vary according to the location of the lymphoma.
• Central nervous system oxygen toxicity: High oxygen levels which affects the central nervous system. The condition can occur during deep dives with fatal consequences.
• Central nervous system protozoal infections: A protozoal infection of the central nervous system (spinal cord or brain). The infection may originate in the central nervous system (primary infection) or may spread from another part of the body (secondary infection). The infection may occur in otherwise healthy individuals or in individuals who have a compromised immune system. Primary protozoal CNS infections include cerebral amebiasis, granulomatous amebic encephalitis and secondary infections include cerebral malaria and cerebral babesiosis.
• Cephalosporin-induced Immune Hemolytic Anemia: Cephalosporin-induced immune hemolytic anemia is a condition where a use of a medication called Cephalosporin triggers the body's immune system to destroy it's own red blood cells which results in anemia.
• Ceptaz - Teratogenic Agent: There is evidence to indicate that exposure to Ceptaz (an antibiotic) during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
• Cerebellar vermis hypoplasia - oligophrenia - congenital ataxia - coloboma - hepatic fibrosis: A very rare syndrome characterized by ataxia, gaps or holes in various eye structures, mental retardation, liver fibrosis and brain abnormalities.
• Cerebral Amyloid Angiopathy, Familial: A rare disorder where abnormal deposits of amyloid in the brain blood vessels causes spasticity, incoordination and dementia. Brain hemorrhage and strokes may also result in severe cases.
• Cerebral cavernous malformations: A rare disorder where a group of small abnormal blood vessels in the brain. These blood vessels become enlarged, irregularly shaped and thin walled. They swell when filled with blood and are then often unable to return to their original shape and the thin walls means that they can leak blood and cause bleeding in the brain. Severity of symptoms depends on the number and location of the lesions.
• Cerebral ventricle neoplasm: A tumor that occurs in the fluid-filled spaces of the brain called the ventricles. Symptoms vary depending on the size and exact location of the tumor and whether it is cancerous or not.
• Ceroid lipofuscinosis, neuronal 2, late infantile type: A rare inherited biochemical disorder involving the progressive accumulation of certain chemicals (lipopigments) in body tissues due to deficiency of an enzyme (protease tri-peptidyl-peptidase) needed to process it.
• Cervical Teratoma: A cervical teratoma is a very rare form of germ cell tumor that occurs in the neck. These tumors usually develop in the fetus and tend to be large and benign even though they grow continually. In rare cases they can occur in adults in which case they tend to be malignant. These tumors can be quite large and cause problems in other neck structures. Sometimes surgery is required in the uterus or during delivery in order to ensure the infant has access to an airway.
• Chagas disease: A parasitic infection caused by the protozoa Trypanosoma cruzi and transmitted by insect bites or blood transfusions. The disease primarily involves the heart and gastrointestinal system.
• Charcot-Marie-Tooth disease, Type 2C: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 2C has an autosomal dominant inheritance and involves a defect in chromosome 12 and involves diaphragm and vocal cord weakness as well as hand and foot problems.
• Chediak-Higashi like syndrome: A rare genetic disorder characterized mainly by albinism (lack of pigmentation). There are three different subtypes of the disorder (I, II and III) each with varying additional features such as immunodeficiency and neurological symptoms. Type 1 involves partial albinism and neurological symptoms, type II involves partial albinism, immunodeficiency and sometimes neurological symptoms and type III involves albinism only.
• Chemical burn: A chemical burn is a burn caused by a chemical. Symptoms vary depending on the chemical, the part of the body affected and the duration of the exposure to the chemical. Rapid first aid following exposure can limit the damage caused by the chemical. Chemical burns can occur when certain chemicals are accidentally swallowed, spilt on the skin, splashed in the eyes or even breathed in the case of chemical gases.
• Chemical burn - airways: Burns to the airways caused by a chemical - usually through inhalation but can also occur through aspiration if the chemical is swallowed. Symptoms vary depending on the type, quantity and strength of the chemical involved as well as the duration of the exposure to the chemical and promptness of treatment measures. Immediate medical attention should be sought if chemical burns to the airways are suspected.
• Chemical burn - ingestion: Burns to the mouth and gastrointestinal system caused by swallowing a chemical. Symptoms vary depending on the type, quantity and strength of the chemical involved as well as the duration of the exposure to the chemical and promptness of treatment measures. Immediate medical attention should be sought if chemical burns to the gastrointestinal system are suspected.
• Chemical burn - inhalation: Burns to the airways caused by a chemical through inhalation. Symptoms vary depending on the type, quantity and strength of the chemical involved as well as the duration of the exposure to the chemical and promptness of treatment measures. Immediate medical attention should be sought if chemical burns to the airways are suspected.
• Chemical burn - skin: Burns to the skin caused by a chemical. Symptoms vary depending on the type, quantity and strength of the chemical involved as well as the duration of the exposure to the chemical and promptness of treatment measures.
• Chemical poisoning - 1,1-Dimethylhydrazine: 1,1-Dimethylhydrazine is a chemical used mainly in jet fuel and rocket fuel, plant growth agent, photography and various other industrial uses. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - 4-Aminopyridine: 4-Aminopyridine is a pesticide used mainly to control bird pests. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - 5,-Methoxy-N,N-Diisopropyltryptamine: 5,-Methoxy-N,N-Diisopropyltryptamine is a chemical used as a designer drug for its hallucinogen and aphrodisiac effects. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Acetic Anhydride: Acetic Anhydride is a chemical used mainly in various industrial processes as well as the production of pharmaceutical products such as aspirin and acetyl salicylic acid. It is also used in the production of heroin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Acetylsalicylic Acid: Acetylsalicylic Acid is also known as aspirin and is primarily used to relieve pain, fever and inflammation. Excessive exposure to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Acrylic acid: Acrylic acid is a chemical used mainly in the production of resins and acrylic acids which are usually used in adhesives and coatings. It is also used in water treatment and in the production of plastics and detergents. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Acrylonitrile: Acrylonitrile is a chemical used mainly in the production of acrylic and modacrylic fibers but also in the production of certain plastics, nylon dyes, drugs and pesticides. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Agrocide: Agrocide is a chemical insecticide used mainly to control scabies or lice as well as other agricultural insect pests. The insecticide is considered moderately toxic to humans and acts as a central nervous system stimulant. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Agronexit: Agronexit is a chemical insecticide used mainly as an agricultural insecticide. The insecticide is considered moderately toxic to humans and acts as a central nervous system stimulant. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Aldrin: Aldrin is a chemical once used mainly in insecticides for crops and as a termite preventative. The chemical can readily be absorbed through the skin. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Amidithion: Amidithion is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Amiton: Amiton is a chemical once used as an insecticide and acaricide - it is no longer in use due to its nerve toxicity. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Ammonium Bifluoride: Ammonium Bifluoride is a chemical used wheel cleaners, herbicides and in the manufacture of magnesium. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Anti-rust products: Anti-rust products contain various chemicals which are toxic if ingested. The ingested chemicals can continue to cause damage to the organs and gastrointestinal lining for weeks after the ingestion and severe cases can result in death. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Anticoagulant rodenticide: Anticoagulant rodenticide is a chemical used to control rodents. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Aparasin: Aparasin Aparasin. The insecticide is considered moderately toxic to humans and acts as a central nervous system stimulant. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Aphtiria: Aphtiria is a chemical insecticide used mainly to control scabies or lice. The insecticide is considered moderately toxic to humans and acts as a central nervous system stimulant. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Athyl-Gusathion: Athyl-Gusathion is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Azinfos-methyl: Azinfos-methyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Azinfosethyl: Azinfosethyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Azinophos-methyl: Azinophos-methyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Azinphos: Azinphos is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Azinphos-ethyl: Azinphos-ethyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Azinphos-methyl: Azinphos-methyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Azinphosmetile: Azinphosmetile is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Azothoate: Azothoate is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Ben-Hex: Ben-Hex is a chemical insecticide used mainly to control scabies. The insecticide is considered moderately toxic to humans and acts as a central nervous system stimulant. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Benhexol: Benhexol is a chemical insecticide used mainly to control scabies or lice. The insecticide is considered moderately toxic to humans and acts as a central nervous system stimulant. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Benoxafos: Benoxafos is a chemical pesticide used as an acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Benzene hexachloride: Benzene hexachloride is a chemical insecticide. The insecticide is considered moderately toxic to humans and acts as a central nervous system stimulant. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Bexol: Bexol is a chemical insecticide used mainly to control scabies or lice. The insecticide is considered moderately toxic to humans and acts as a central nervous system stimulant. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Borates: Borate is a chemical used in a wide variety of products - herbicides, paints, insecticides, rodenticides and various personal products such as skin creams, toothpastes and powders. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Boric Acid: Boric Acid is a chemical used mainly in foods (preservative, emulsifier, neutralizer), antiseptics, pesticides and contact lens cleaners. Ingestion and other exposures to the chemical can cause various symptoms. Application of boric acid directly to damaged skin can cause the chemical to be absorbed rapidly into the body and lead to death. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Brodifacoum: Brodifacoum is a chemical used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Bromadiolone: Bromadiolone is a chemical used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Bromethalin: Bromethalin is a chemical used mainly in rodenticides. The chemical is toxic to the human nerve system. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Bromoform: Bromoform is a chemical with limited industrial uses but is used as a laboratory chemical and can be present in treated water. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Bromophos: Bromophos is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Bromophos-ethyl: Bromophos-ethyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Butyl Alcohol: Butyl alcohol is a chemical used mainly in solvents and in pharmaceutical manufacturing processes. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Butylamines: Butylamines are chemicals used in a variety of manufacturing processes such as in the production of pesticides, pharmaceuticals, plastics, dyes, textiles and in leather tanning and photography. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Cadusafos: Cadusafos is a chemical pesticide used as an insecticide and nematicide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Calcium Polysulfide: Calcium polysulfide is a chemical used mainly in antifungal treatments for trees. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Calcium hypochlorite: Calcium hypochlorite is a chemical used mainly in bleaching products, fungicides, algicides, disinfectants and deodorants. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Carbaryl: Carbaryl is a carbamate pesticide used mainly as an insecticide and acaricide. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Carbon Disulfide: Carbon Disulfide is a chemical used mainly in corrosion inhibitors, cold and nickel plating, photography applications and as a solvent in gums and resins. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Carbon Tetrachloride: Carbon tetrachloride is a chemical used mainly in grain fumigants, insecticides and in the production of fluorocarbons. Ingestion and other exposures to the chemical can cause various symptoms. The chemical is readily absorbed through the skin. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Carbophenothion: Carbophenothion is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Chloresene: Chloresene is a chemical insecticide used mainly to control scabies or lice. The insecticide is considered moderately toxic to humans and acts as a central nervous system stimulant. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Chlorfenvinphos: Chlorfenvinphos is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Chlorine: Chlorine is a chemical used mainly in bleaches, water disinfectants and in pulp mills. Ingestion and other exposures to the chemical can cause various symptoms. Chlorine is very corrosive and extensive damage to body tissues can result. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Chloropyrifos: Chloropyrifos is a chemical pesticide used as an insecticide, nematicide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Chlorpyrifos methyl: Chlorpyrifos methyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Clinitest tablet: Clinitest tablet are used to test sugar levels in urine. The tablets contain various chemicals (copper sulfate, sodium hydroxide, sodium carbonate) and eating them can cause serious symptoms. The chemicals cause damage to the gastrointestinal lining and the damage may continue for weeks after the poison was ingested. Death can result in severe cases. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Cresols: Cresols are a group of chemicals that occur naturally in mammals and various plants. It is also manufactured and used in the production of disinfectants, deodorizers and pesticides. Ingestion and other exposures to the chemical can cause various symptoms. The chemical is readily absorbed through the skin. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Cresylic acid: Cresylic acids are a group of chemicals that are used as solvents and in the manufacture of various products such as deodorants, disinfectants, pesticides, glues, paints, herbicides, pharmaceuticals as well as others. Ingestion and other exposures to the chemical can cause various symptoms. The chemical is readily absorbed through the skin. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Cyanthoate: Cyanthoate is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Cyclohexanone: Cyclohexanone is a chemical used mainly as an industrial solvent, in processes involving oxidative reactions and in the manufacture of certain resins, nylons, insecticides, herbicides, paints, varnish, polishes, degreasers and pharmaceuticals. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Cyclohexylamine: Cyclohexylamine is a chemical used industrial and household applications: pesticides, dry-cleaning soaps, plasticizers, textile chemicals, artificial sweeteners, dyes and corrosion inhibitors. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Cypermethrin: Cypermethrin is a widely used insecticide and acaricide. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - DDD: DDD is a chemical used mainly as a pesticide. Ingestion and other exposures to the chemical can cause various symptoms. The chemical may be readily absorbed through the skin. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - DDT: DDT is a chemical used mainly as a pesticide. Ingestion and other exposures to the chemical can cause various symptoms. The chemical may be readily absorbed through the skin. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Demeton: Demeton-S is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Demeton-O: Demeton-O is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Demeton-O-methyl: Demeton-O-methyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Demeton-S-methyl: Demeton-S-methyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Demeton-S-methylsulphon: Demeton-S-methylsulphon is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Demeton-methyl: Demeton-methyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Deoderant: Deoderants contain various chemicals which can cause serious symptoms if sufficient quantities are ingested. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Depilatories: Depilatories are used to remove hair from parts of the body. They contain various chemicals which can cause serious symptoms if sufficient quantities are ingested. The chemicals cause damage to the gastrointestinal lining and the damage may continue for weeks after the poison was ingested. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Dialifos: Dialifos is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Diazinon: Diazinon is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Dichlorvos: Dichlorvos is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Dicrotophos: Dicrotophos is a toxic insecticide. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Dieldrin: Dieldrin is a chemical used mainly to prevent termite infestations. Ingestion and other exposures to the chemical can cause various symptoms. This chemical may be absorbed readily through the skin. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Dimethoate: Dimethoate is a chemical pesticide used as an insecticide, nematicide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Dioxathion: Dioxathion is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Disulfiram: Disulfiram is a drug used mainly to manage alcoholism. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Disulfoton: Disulfoton is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Endothion: Endothion is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Ethion: Ethion is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Ethoate-methyl: Ethoate-methyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Ethoprophos: Ethoprophos is a chemical pesticide used as an insecticide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Ethyl-guthion: Azinphos-ethyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Ethylamine: Ethylamine is a chemical used mainly in the manufacture of dyes, rayon, rocket propellant, as a fuel additive and in leather-tanning and cellulose treatment. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Ethylbenzene: Ethylbenzene is a chemical used mainly in paint thinners, fuels, asphalt, degreasers, manufacture of various as products and as a solvent. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Ethylene Glycol: Ethylene Glycol is a chemical used mainly in antifreeze, coolants and as a solvent. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. Symptoms tend to occur in three phases: the first 12 hours involves inebriation, seizuresand brain swelling; the second and third day involves deterioration of lung and heart function and the third stage involves kidney damage and possibly failure. Death can occur during any of the stages.
• Chemical poisoning - Ethylene Glycol Dinitrate: Ethylene Glycol Dinitrate is a chemical used mainly in the manufacture of commercial dynamite and blasting gelatin. The chemical may be absorbed readily through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Etrimfos: Etrimfos is a chemical insecticide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Fenchlorphos: Fenchlorphos is a chemical insecticide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Fenitrothion: Fenitrothion is a chemical insecticide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Fensulfothion: Fensulfothion is a chemical pesticide used as an insecticide and nematicide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Fenthion: Fenthion is a chemical pesticide used as an insecticide and avicide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Fluoridated toothpaste: Fluoridated toothpaste contains fluoride and various other chemicals which can cause serious symptoms if sufficient quantities are swallowed. As little as half a tube of children's paste can cause death in a 2 year old child and a whole tube can cause death in a 9 year old child. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Fonophos: Fonophos is a chemical insecticide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Formaldehyde: Formaldehyde is a chemical used mainly in blues, lacquers, fireproofing, electrical insulation, leather tanning products and embalming. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Formothion: Formothion is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Furniture polish: Furniture polish contains chemicals (hydrocarbons) which can cause serious symptoms if ingested. The ingested chemicals can continue to cause damage to the organs and gastrointestinal lining for weeks after the ingestion and severe cases can result in death. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Guthion (ethyl): Guthion (ethyl) is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - HCH-gamma: HCH-gamma is an insecticide which is considered moderately toxic to humans and acts as a central nervous system stimulant. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Heptenophos: Heptenophos is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Hexachlorocyclohexane (gamma): Hexachlorocyclohexane (gamma) is an insecticide which is considered moderately toxic to humans and acts as a central nervous system stimulant. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Hydrazine: Hydrazine is a chemical used mainly in rocket fuel, photography, laboratory chemical, corrosion inhibitor, mirror silvering and in the production of pharmaceuticals and pesticides. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Iodofenphos: Iodofenphos is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Isofenphos: Isofenphos is an insecticide. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Jet Fuel-4: Jet Fuel-4 is an aviation turbine fuel used by the US military. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Jewelry cleaner: Jewelry cleaner contains various chemicals which can cause serious symptoms if ingested or other types of exposure occurs. The chemicals cause damage to the gastrointestinal lining and the damage may continue for weeks after the poison was ingested. Death can result in severe cases. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Lacquer: Lacquer contains various chemicals which can cause serious symptoms if ingested or other types of exposure occurs. The chemicals cause damage to the gastrointestinal lining and the damage may continue for weeks after the poison was ingested. Death can result in severe cases. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Lewisite: Lewisite is a very poisonous gas which has the potential to be used in chemical warfare due to its deadly effects. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Lighter fluid: Lighter fluid contains various chemicals which can cause serious symptoms if ingested or other types of exposure occurs. The chemicals cause damage to the gastrointestinal lining and the damage may continue for weeks after the poison was ingested. Death can result in severe cases. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Lindane: Lindane is a chemical used mainly as an agricultural insecticide but also as a treatment of lice and scabies infestations. The insecticide is considered moderately toxic to humans and acts as a central nervous system stimulant. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Lysergic Acid Diethylamide: Lysergic Acid Diethylamide is a hallucinogenic drug which is often misused. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Malathion: Malathion is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Mecarbam: Mecarbam is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Metal polish: Metal polish contains various chemicals which can cause severe symptoms if ingested or other forms of exposure occur. The chemicals cause damage to the gastrointestinal lining and the damage may continue for weeks after the poison was ingested. Death can result in severe cases. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Metaldehyde: Metaldehyde is a chemical used mainly as a molluscicide, in heating fuel and in fire lighters. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Methacrifos: Methacrifos is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Methamidophos: Methamidophos is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Methidathion: Methidathion is a chemical insecticide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Methiocarb: Methiocarb is a toxic pesticide. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Methomyl: Methomyl is a carbamate pesticide used mainly as an insecticide. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Methyl Bromide: Methyl Bromide is a chemical used mainly in insecticides, fire extinguishers, wool degreasers and oil extraction. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Methyl Isocyanate: Methyl Isocyanate is a chemical used mainly in herbicides and pesticides. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Methyl Mercaptan: Methyl Mercaptan is a chemical used mainly in the production of plastic, pesticides and jet fuel. It is also used in certain toxic gases to give them a detectable odor. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Methyl parathion: Methyl parathion is a chemical used mainly as an insecticide for various crops. Ingestion and other exposures to the chemical can cause various symptoms. The chemical may be absorbed through the skin. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Methylene Chloride: Methylene Chloride is a chemical used mainly in paint removers, nail polish remover, fumigants and fire extinguishers. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Metiltriazotion: Metiltriazotion is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Mevinphos: Mevinphos is a chemical insecticide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Mineral-Based Crankcase Oil: Mineral-Based Crankcase Oil is a chemical used mainly as a fuel . Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Monocrotophos: Monocrotophos is a chemical insecticide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Naphthalene: Naphthalene is a chemical used mainly as a moth repellant, toilet deodorizer and the manufacture of other chemicals. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Nitrogen Dioxide: Nitrogen Dioxide is a chemical which has industrial applications but is also an air pollutant formed by burning fossil fuels such as gas, oil and coal as well as vehicle exhaust and industrial byproduct. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Nitroglycerin: Nitroglycerin is a chemical used mainly in the manufacture of explosives, dynamite, rocket propellant and smokeless powders. The chemical is readily absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Omethoate: Omethoate is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Oven Cleaners: Oven cleaners contain toxic chemicals which can cause serious symptoms on exposure. Severe gastrointestinal burns can be caused by ingesting oven cleaner. The burns can lead to perforation which involves a high risk of death. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Oxydeprofos: Oxydeprofos is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Oxydisulfoton: Oxydisulfoton is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Paramethoxyamphetamine: Paramethoxyamphetamine is used as a recreational hallucinogenic drug. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Parathion: Parathion is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Parathion Methyl: Parathion Methyl is a chemical insecticide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Pentachlorophenol: Pentachlorophenol is a chemical used mainly in fungicides, herbicides, insecticides, molluscicides, algicides and bactericides. It is commonly used as a wood preservative. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Phencyclidine: Phencyclidine is often used as an illegal recreational drug. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Phenkapton: Phenkapton is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Phorate: Phorate is a chemical pesticide used as an insecticide, nematicide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Phosalone: Phosalone is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Phosdrin: Phosdrin is a toxic pesticide. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Phosmet: Phosmet is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Phosphamidon: Phosphamidon is a chemical pesticide used as an insecticide and nematicide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Phosphine: Phosphine is a chemical used mainly in pesticides and rodenticides. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Phoxim: Phoxim is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Pine Oil: Pine Oil is a chemical used mainly as a disinfectant or cleaning agent. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Pirimiphos-methyl: Pirimiphos-methyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Pool Cleaners: Pool Cleaners contain various chemicals (mainly chlorine) which can cause serious symptoms if sufficient quantities are swallowed. The chemicals are very damaging to the mucosal linings in the body. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Primiphos methyl: Primiphos methyl is a chemical insecticide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Profenofos: Profenofos is a toxic pesticide. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Prothidathion: Prothidathion is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Prothoate: Prothoate is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Pyrimitate: Pyrimitate is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Quinalphos: Quinalphos is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Quintiofos: Quintiofos is a chemical pesticide used as an acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Rotenone: Rotenone is a naturally occurring chemical found in certain plants (Derris and Lonchocarpus sp.). It gives the plant insecticidal and pesticidal properties and is hence utilized commercially as an insecticide. Ingestion and other exposures to the chemical can cause various symptoms. Inhalation tends to cause more severe symptoms than ingestion. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Sophamide: Sophamide is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Strychnine: Strychnine is used as a rodenticide. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Sulfotep: Sulfotep is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Terbufos: Terbufos is a chemical pesticide used as an insecticide and nematicide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Tetraethyl Pyrophosphate: Tetraethyl Pyrophosphate is a toxic pesticide. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Thallium: Thallium is an element used for such things as electronic devices, selenium rectifiers, gamma radiation detection apparatus, transmission equipment and infrared radiation detection. It is also used as a catalyst in various manufacturing processes. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Thiometon: Thiometon is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Thorium: Thorium is an element used mainly as a nuclear power source and in magnesium alloys, electronic tubes, light filaments and electrodes. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Tolclofos methyl: Tolclofos methyl is a chemical insecticide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Triazophos: Triazophos is a chemical pesticide used as an insecticide, nematicide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Triazotion: Triazotion is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Trichlorfon: Trichlorfon is an insecticide used mostly in crops. It is considered motderately toxic to humans. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Triethylene Glycol: Triethylene Glycol is a chemical used mainly in brake fluid. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Trifenfos: Trifenfos is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - Uranium: Uranium is an element used mainly in commercial nuclear power plants. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical poisoning - Vamidothion: Vamidothion is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The chemical may be absorbed through the skin.
• Chemical poisoning - gamma-HccH: Gamma-HccH is an insecticide which is considered moderately toxic to humans and acts as a central nervous system stimulant. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chemical-induced cardiovascular disease: Chronic exposure to certain chemicals can cause cardiovascular disease. For example, exposure to Carbon disulfide can lead to heart disease and carries a risk of premature death as a result. Chronic exposure to these sort of chemicals is most likely to occur in a work environment.
• Cherry laurel seed poisoning: Wild cherry seeds contain a chemical called amygdalin which breaks down into cyanide in the human body. The toxic chemicals are not released if the seed remains intact and therefore poisoning usually occurs if the seeds are crushed and eaten. Accidental ingestion is very unusual. Wild cherry plants grow mainly in eastern Europe, Western Asia and Britain.
• Cherry seed poisoning: Cherry seeds contain a chemical called amygdalin which breaks down into cyanide in the human body. The toxic chemicals are not released if the seed remains intact and therefore poisoning usually only occurs if the seeds are crushed and eaten. Accidental ingestion is very unusual.
• Childhood asthma: Childhood asthma is a type of asthma that occurs during childhood. Asthma involves constriction and inflammation of the airways. The severity of symptoms is variable. The asthma may be triggered by allergens, pollution, viral infections and many other factors.
• Childhood liver cancer, primary: Cancer that develops in the tissue of the liver in children.
• Chirodropidae poisoning: Chirodropidae are jellyfish-like marine organisms found mainly in the Indian and Pacific Oceans. They can deliver a painful sting which can be life-threatening in some cases. The box jellyfish, Irukundji jellyfish and some sea wasps are all members of this class.
• Chlorophacinone rodenticide poisoning: Chlorophacinone is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Chokecherry seed poisoning: Chokecherry seeds contain a chemical called amygdalin which breaks down into cyanide in the human body. The toxic chemicals are not released if the seed remains intact and therefore poisoning usually occurs if the seeds are crushed and eaten. Accidental ingestion is very unusual. Chokecherry plants grow mainly in Northern America.
• Choking: Sensation of blockage or inability to breathe.
• Cholera: An acute bacterial disease transmitted through food or water contaminated with human faeces. The intestinal infection is caused by the bacterium Vibrio cholerae.
• Cholestasis, progressive familial intrahepatic 2: A rare inherited condition where bile is unable to drain from the liver where it builds up and causes progressive liver damage. The condition has an early onset and usually leads to end-stage liver disease by the end of the second decade. The various types of this condition differ in the origin of the genetic defect (liver-specific ATP-binding cassette transporter on chromosome 2q24). Type 2 is also associated with an increased risk of liver cancer in the first few years of life.
• Cholestasis, progressive familial intrahepatic 3: A rare inherited condition where bile is unable to drain from the liver where it builds up and causes progressive liver damage. The condition has an early onset and usually leads to end-stage liver disease by the end of the second decade. The various types of this condition differ in the origin of the genetic defect (liver-specific ATP-binding cassette transporter on chromosome 2q24). Type 2 is also associated with an increased risk of liver cancer in the first few years of life.
• Cholesterol and lipids: Levels of blood or urine cholesterol or lipids as a symptom
• Cholesterol pneumonia: Lung inflammation caused by cholesterol.
• Chondrodysplasia punctata lethal neonatal: A rare skeletal disorder which results in the infant's death before or soon after birth. Symptoms include a variety of severe skeletal abnormalities and an enlarged head.
• Chondrodysplasia, Grebe type: A rare genetic disorder characterized by dwarfism and various limb deformities.
• Chondrodystrophia calcificans congenita: A rare genetic disorder characterized by growth deficiency, short limbs, large skin pores, sparse hair and other abnormalities.
• Chondrodystrophia punctata, autosomal dominant: A rare genetic disorder characterized by growth deficiency, short limbs, large skin pores, sparse hair and other abnormalities.
• Choroid plexus calcification with mental retardation: A form of mental retardation associated with calcification of the choroids plexus which is the part of the brain involved in making cerebrospinal fluid.
• Chromophil renal cell carcinoma: A type of kidney tumor where the cells that make up the tumor take up dye readily during pathology testing.
• Chromophobe renal cell carcinoma: A rare type of kidney tumor. The cells that make up the tumor tend to be clear and do not readily take up dye during pathology analysis. Metastasis often only occurs late in the course of the disease and surgical removal usually leads to a good prognosis.
• Chromosome 1, 1p36 deletion syndrome: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as heart problems, mental retardation, developmental delay, facial dysmorphism and short stature. The symptoms are variable depending on the exact location of chromosomal deletion.
• Chromosome 1, Partial Trisomy: A rare genetic disorder where part of the genetic material from chromosome 1 is duplicated so there are three copies in the body's cells rather than the normal two copies. The type and severity of symptoms is variable depending on the size and location of the genetic material duplicated.
• Chromosome 1, duplication 1p21 p32: A rare chromosomal disorder where duplication of a portion of chromosome 1 causes various abnormalities such as short stature, newborn or fetal death, small head, undescended testes and various facial abnormalities.
• Chromosome 1, monosomy 1q32 q42: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as fetal or newborn death, facial dysmorphism, short stature, finger defects and various other anomalies.
• Chromosome 1, pter-p36: A very rare chromosomal disorder where the end portion of the short arm of chromosome 1 is missing. The type and severity of symptoms is variable.
• Chromosome 1, trisomy 1q32 qter: A rare chromosomal disorder where duplication of a portion of chromosome 1 causes various abnormalities such as retarded fetal growth, facial anomalies, mental retardation, stillbirth, heart defects and finger and toe abnormalities.
• Chromosome 10p terminal deletion syndrome: A very rare syndrome caused by a chromosomal defect (10p terminal deletion) and can result in a variety of malformations that are similar to DiGeorge syndrome and velocardiofacial syndrome.
• Chromosome 12, trisomy 12q: A rare chromosomal disorder where there are three copies of the long arm (q) of chromosome 12 rather than the normal two resulting in various abnormalities. In most cases, death occurs during infancy. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is duplicated.
• Chromosome 12q duplication syndrome: A rare chromosomal disorder where there are three copies of the long arm (q) of chromosome 12 rather than the normal two resulting in various abnormalities. In most cases, death occurs during infancy.
• Chromosome 13q partial deletion: A rare chromosomal disorder where part of the long arm (q) of chromosome 13 is deleted resulting in various physical, neurological and developmental abnormalities. The type and severity of symptoms is determined by the amount and location of the deleted genetic material.
• Chromosome 14 trisomy: A rare chromosomal disorder involving duplication of genetic material from chromosome 14 resulting in various abnormalities. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is duplicated.
• Chromosome 15q duplication syndrome: A rare chromosomal disorder involving an extra copy of genetic material from the long arm of chromosome 15. The type and severity of symptoms are determined by the amount and location of the duplicated genetic material.
• Chromosome 15q, trisomy: A rare chromosomal disorder involving an extra copy of genetic material from the long arm of chromosome 15. The type and severity of symptoms are determined by the amount and location of the duplicated genetic material.
• Chromosome 16q, partial duplication: A rare chromosomal disorder involving an extra copy of genetic material from the long arm of chromosome 16. The type and severity of symptoms are determined by the amount and location of the duplicated genetic material. Severe cases often result in spontaneous abortion or infant death.
• Chromosome 2, trisomy 2q: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 2 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material.
• Chromosome 21, monosomy 21q22: A rare chromosomal disorder where a portion of the long arm of chromosome 21 is deleted.
• Chromosome 22, trisomy: A very rare disorder where there is an extra copy of chromosome 22 in all the body cells. The condition is usually fatal soon after birth or during the fetal stage.
• Chromosome 2q duplication syndrome: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 2 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material.
• Chromosome 3 duplication syndrome: There is very little information on this very rare genetic condition where there is an extra copy of chromosome 3 in the body's cells. The condition is considered lethal.
• Chromosome 4 short arm deletion: A rare chromosomal disorder where part or all of the short arm (p) of chromosome 4 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
• Chromosome 7, Monosomy: A rare chromosomal disorder where there is one copy of the genetic material in chromosome 7 rather than the normal two. The deletion of this chromosome if often associated with myelodysplastic syndromes and myeloid leukemia. The condition usually has a poor prognosis. Other defects may also be present in some cases.
• Chromosome 7, trisomy 7q: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 7 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material.
• Chromosome 8, mosaic trisomy: A very rare chromosomal disorder where there is an extra copy of chromosome 8 in some of the body's cells. Some cases with this chromosomal abnormality have no clinical symptoms. The presence of abnormalities in some cases is dependent on which body cells contain the chromosomal defect.
• Chromosome 9/mosaic: A rare chromosomal disorder where chromosome 9 is duplicated in some of the body's cells resulting in various abnormalities determined by the type and number of cells that contain the extra genetic material.
• Chronic Myeloproliferative Disease, Unclassified: A form of blood disorder characterized by the abnormal proliferation of myeloid precursors in the bone marrow. This category refers to cases of myeloproliferative disease which don't fit into any of the other specific type of myelproliferative diseases.
• Chronic Neutrophilic Leukemia: A rare form of leukemia characterized by excessive levels of mature neutrophils.
• Chronic adult T-Cell leukemia: A form of blood cancer affecting the T-cells which make up the body's immune system. The disease is caused by the HTLV-1 virus (human T-cell leukemia virus) which causes the proliferation of abnormal T-cells. The virus can be transmitted sexually and may lay dormant for decades. There are four subtypes: acute, chronic, lymphoma and smoldering. The acute and lymphoma subtypes have the poorest prognosis. The acute form tends to progress relatively slowly and generally responds better to treatment than the other subtypes.
• Chuifong tokuwan-induced lead poisoning: Chuifong tokuwan is a folk remedy used mainly by Asian people to arthritis and other pain. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Ciclosporin - Teratogenic Agent: There is evidence to indicate that exposure to Ciclosporin (an immunosuppressant drug) during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
• Citalopram toxicity: The toxic reaction of the body to the substance, possibly via allergic reaction or overdose.
• Classic galactosemia: Rare serious genetic defect in galactose metabolism.
• Classical Potter syndrome: A term that describes the physical appearance that occurs when kidney disease results in a reduced volume of amniotic fluid. In the classical type, both kidneys are absent.
• Claviceps purpurea poisoning: Claviceps purpurea is a type of fungus that can contaminate grains such as rye, wheat, oats and barely. Ingestion of contaminated foods can cause poisoning with the severity of symptoms varying depending on the amount consumed.
• Clear cell renal cell carcinoma: A type of kidney tumor where the cells that make up the tumor are clear.
• Cleft palate - cardiac defect - genital anomalies - ectrodactyly: A very rare syndrome characterized by variable symptoms including cleft palate, heart defects, genital anomalies and hand and foot malformations.
• Clonorchiasis: Infection with the Chinese liver fluke called Clonchorchis sinensis. Infection usually results from ingesting contaminated fish and crayfish. The infection primarily affects the liver as the flukes tend to occupy the biliary ducts of the liver. Recurring infections can cause more severe symptoms. Infection with this fluke is endemic in Asia but can occur occasionally in countries such as the US though the source of contamination is food from Asia.
• Clostridium sordellii: Clostridium sordellii is a rare bacterium that can cause infections such as pneumonia, arthritis, peritonitis and endocarditis. It is most often associated with childbirth, trauma, medically induced abortions, injection drug use and routine gynecological procedures. Death is not uncommon with this type of infection. In rare cases it can cause toxic shock syndrome.
• Clotting symptoms: Symptoms affecting the blood's ability to clot
• Cloverleaf skull micromelia thoracic dysplasia: A rare disorder characterized by a cloverleaf skull deformity, small limbs and bone abnormalities of the chest and spine. The disorder is lethal.
• Clupeotoxism: A potentially fatal condition caused by eating fish such as herrings and anchovies from the Clupeidae family of fish. Severe poisoning can result in death within half an hour of ingestion. Outbreaks have been reported in the Caribbean Sea and the Indian-Pacific area.
• Coarctation of aorta dominant: A rare inherited birth defect where the heart blood vessel called the aorta has a narrowed area which affects blood flow. The degree of constriction is variable which mild cases asymptomatic until adulthood. The poor blood flow to the lower body gives results in it appearing less developed than that upper body.
• Coastal leucothoe poisoning: The coastal leucothoe is an evergreen shrub which bears small clusters of bell-shaped, white flowers in the apex of the leaves. It also bears small capsulated fruit. The leaves and flower nectar contain a chemical called andromedotoxin which is very toxic and can cause death if sufficient quantities are eaten.
• Cobalt-induced myocardial injury: Exposure to cobalt has the potential to cause damage to the heart muscle. Severe damage can result in chronic heart problems or even death in severe cases. Cobalt exposure is most likely to occur in an occupational setting.
• Cobra poisoning: The Cobra is a poisonous snake which can be found in Africa, Asia and other parts of the world. Some cobras are able to spit venom into the victims eye and cause serious symptoms.
• Cocaine abuse: Stimulant drug with various effects
• Cocaine addiction: An uncontrollable desire to use cocaine on a regular basis. Chronic cocaine use can lead to dependency in as little as two weeks. Frequent use leads to an increased tolerance to the drug so higher and higher doses are required to achieve the desired euphoric feeling.
• Cocaine overdose: Cocaine is an illegal and highly addictive recreational drug. Excessive doses of the drug can result in various symptoms and even death in severe cases.
• Cocaine-induced hypertension: Cocaine-induced hypertension is high blood pressure caused by use of cocaine. Patients with an existing history of hypertension may suffer further blood pressure increases while taking cocaine and this can be serious. Severity of symptoms varies amongst patients depending on their susceptibility, underlying health and duration of cocaine use.
• Coconut crab poisoning: The coconut crab is commonly found and eaten as a delicacy in the Indo-Pacific region. These crabs can contain toxic chemicals which can cause severe poisoning in humans if eaten. The toxicity of these crabs is believed to be derived from the ingestion of certain toxic ocean plants. The best way to avoid poisoning is to not eat these crabs at all.
• Codeine overdose: Codeine is a prescription drug mainly used to treat pain. Excessive doses of the drug can result in various symptoms and even death in severe cases.
• Coenzyme Q cytochrome c reductase deficiency of: A rare genetic defect where an enzyme deficiency (CoQ-Cytochrome C reductase) disrupts cellular processes. Any of a variety of the components of the enzyme may be missing or defective and hence the clinical presentation and severity may vary. The deficiency may result in a variety of symptoms and conditions of variable severity such as cardiomyopathy, fatal infant conditions and Leber's myopathy.
• Colavita-Kozlowski syndrome: A very rare syndrome characterized by dwarfism and resulting in death at birth or in the weeks following birth.
• Colchicine poisoning: Ingestion of toxic quantities of colchicines. Colchicine is primarily used as a medicinal theapy for conditions such as gout and familial Mediterranean fever, scleroderma, secondary amyloidosis and pericarditis. The chemical is a natural chemical found in a plant called meadow saffron and ingestion of the plant can also result in poisoning. The plant is found in the northern parts of the world.
• Cold Autoimmune Hemolytic Anemia: Cold autoimmune hemolytic anemia is a condition where the body's immune system triggers the production of antibodies against the body's own red blood cells. The red cells are destroyed at an abnormally rapid rate which leads to anemia. Cold haemolytic anemia is characterized by the fact that the abnormal destruction of red blood cells is more active when the patient is exposed to cold temperatures. The severity of the condition varies depending on the underlying cause. The condition may develop gradually or occur suddenly and cause serious symptoms.
• Colibacillosis: Infection with a bacteria called Escherichia coli. Infection can cause severe diarrhea or septicemia. The bacteria can also produce toxins which can affect other parts of the body also. Infections can occur anywhere in the world but some developing countries have endemic areas. Transmission can occur contaminated animal products or contact with infected cats and dogs.
• Collagenous celiac disease: Collagenous celiac disease is used to describe progressive celiac disease characterized by the presence of a layer of collagen (scarring) in the intestinal layers. This form of celiac disease usually fails to respond to treatments such as gluten-free diets. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The condition usually fails to respond to treatment and has a poor prognosis.
• Collapsed lung: Deflation of all or part of one lung
• Collecting duct carcinoma: A rare, aggressive type of kidney cancer that arises from the kidney collecting ducts. The cancer cells can form irregular tubes.
• Colloid cysts of third ventricle: A rare type of benign brain tumor. In rare cases the tumor can obstruct the flow of fluid in the brain and cause hydrocephalus (buildup of fluid in the brain). Untreated hydrocephalus can lead to death.
• Colonic malakoplakia: A rare form of inflammatory disease that occurs in the colon and occurs mainly in immunocompromised people. The severity of the disorder can vary from asymptomatic to intestinal obstruction and even death in rare cases.
• Comly syndrome: High blood levels of methemoglobin due to drinking water from wells which have a high nitrate concentration. It is most often seen in babies who have their formula made up using well water. The disorder may also occur in infants who are fed high nitrat food such as eggplant, spinach, beets and green beans. Infants who are less than three months old lack sufficient enzymes to prevent the problem.
• Common poppy poisoning: The common poppy is most commonly associated with cultivation for it's content of opium which is used as an illegal recreational drug. It is illegal to cultivate the plant. However, the plant is legitimately grown in some areas in order to produce medicinal drugs such as morphine, codeine and noscapine. The plant (especially the fruit) contains chemicals (alkaloids, morphine etc) which are very toxic and can cause death if sufficient quantities are eaten. The seeds from the plant are edible and are often used as toppings on breads and cakes.
• Compartment syndrome: compartment syndrome involves the compression of nerves and blood vessels within an enclosed space. This leads to impaired blood flow and muscle and nerve damage
• Complement component deficiency: Complement components are a part of the immune defense system involved in destroying and removing invading pathogens such as bacteria. A deficiency of the complement components can affect the ability of the body's immune system to function properly. The disorder which can be partial or complete and may be inherited or acquired. The severity of the symptoms is determined by which complement component (there are at least 30 of them) is deficient and whether the deficiency is partial or complete.
• Complete Trisomy 18 syndrome: Complete Trisomy 18 syndrome is the most severe form of Edwards syndrome and involves an extra copy of chromosome 18 in all of the body cells. This severe form causes mental retardation and numerous physical defects that often cause death before birth or during infancy.
• Complex 1 mitochondrial respiratory chain deficiency: A rare genetic defect where an enzyme deficiency (NADH CoQ) disrupts cellular processes and causes various organic acid disorders. Any of a variety of the components of the enzyme may be missing or defective and hence the clinical presentation and severity may vary. Presentation may range from infantile death to various disorders such as Leigh's disease, Parkinson's disease and cardiomyopathy.
• Complex 5 mitochondrial respiratory chain deficiency: A rare genetic defect where an enzyme deficiency (ATP synthetase) disrupts cellular processes. Any of a variety of the components of the enzyme may be missing or defective and hence the clinical presentation and severity may vary. The deficiency may result in a variety of symptoms and conditions of variable severity such as Leber's myopathy, Leigh syndrome, cardiomyopathy and NARP (neuropathy, ataxia, retinitis pigmentosa).
• Cone shell poisoning: A number of species of cone shells are capable of envenomating humans. The toxin is a neurotoxin and thus primarily affects the nervous system. Cone shells are found mainly in shallow waters of the Indian and Pacific oceans. The toxicity varies amongst species with some delivering a benign stink whereas others are capable of causing death. The cone snails a proboscis on the end of which is a poison-filled barb.
• Congenital Hemidysplasia with Ichthyosiform erythroderma and Limbs Defects: A rare genetic disorder characterized by unilateral hypomelia, underdeveloped skin and heart defects.
• Congenital adrenal hyperplasia: A condition where excessive secretion of adrenocortical androgens cause a somatic masculization or ?virilization? effect on a fetus or baby. Symptoms in girls may include masculization of sex organs, low voice, acne, amenorrhea and masculine hair distribution and muscle growth. Symptoms in boys include enlarged penis, small testes. Children with the condition are usually taller than average but develop into short adults. Also called adrenogenital syndrome or adrenal virilism.
• Congenital aneurysms of the great vessels: A bulge in one of the main blood vessels in the body - pulmonary artery, pulmonary veins, vena cava and aorta. The condition is generally asymptomatic unless the aneurysm becomes very large or bursts which can result in rapid death depending on the location of the aneurysm.
• Congenital brain dysgenesis due to glutamine synthetase deficiency: A rare genetic metabolic disorder characterized by a deficiency of the glutamine synthase enzyme. This results in a lack of glutamine in the serum, urine and brain and spinal fluid. The condition results in severe brain malformations and infant death within weeks of birth.
• Congenital cardiovascular malformations: The abnormal development of heart blood vessels. Specific examples of this condition includes hypoplastic left heart syndrome, coarctation and tricuspid atresia.
• Congenital chloride diarrhea: A rare birth disorder where the intestines don't absorb electrolytes properly (especially chloride) which leads to electrolyte imbalance which is potentially fatal if untreated. Symptoms often start while the infant is still inside the womb.
• Congenital disorder of glycosylation type 1H: Congenital disorders of glycosylation is a group of very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type Ih is caused by a defect on chromosome 11pter-p15.5 and involves the gene for a particular enzyme (dolichyl-P-glucose:Glc-1-Man-9-GlcNAc-2-PP-dolichyl-alpha-3-glucosyltransferase).
• Congenital disorder of glycosylation type 1M: Congenital disorders of glycosylation is a group of very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type Im is caused by a defect on chromosome 9q34.11 and involves a defect in the TMEM15 gene.
• Congenital disorder of glycosylation type 1X: Congenital disorder of glycosylation is a rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1X also involves thrombocytopenia with normal levels of phosphomannomutase and phosphomannose isomerase. This form of the condition is severe and results in death during infancy.
• Congenital disorder of glycosylation type 2B: A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 2B has glucosidase I enzyme defect.
• Congenital disorder of glycosylation type 2F: Congenital disorders of glycosylation is a group of very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type IIf is caused by a defect on chromosome 6q25.16q15 and involves a defect on the gene for CMP-sialic acid transporter.
• Congenital generalized fibromatosis: A rare disorder where a number of noncancerous tumors form just about any part of the body.
• Congenital heart block: A rare congenital heart disease where a slowed heart rate is caused by defects in the heart conduction system. The condition is usually asymptomatic and harmless but in severe cases (complete AV block) various symptoms and sudden death may occur.
• Congenital herpes simplex: An infant born with a herpes simplex infection transmitted through the mother. The infection may be localized or involve various internal organs and even the central nervous system in which case death can occur.
• Conn Syndrome-induced hypertension: Conn Syndrome-induced hypertension is high blood pressure associated with Conn Syndrome. It results from excessive production of a hormone called aldosterone by the adrenal glands. The high blood pressure often responds poorly to the usual medications. Death can result in severe cases.
• Conn's adenoma: An uncommon (but possible highly underdiagnosed) condition characterized by the excessive production of a hormone called aldosterone by the adrenal gland. The condition may result from the presence of an adrenal adenoma. The severity of the condition is variable with some patients simply suffering high blood pressure and no other symptoms. Due to the high degree of variation in presenting symptoms, the condition may be frequently underdiagnosed or misdiagnosed.
• Conn's syndrome: An adrenal gland disorder where excess aldosterone hormone is produced resulting in symptoms such as headache, fatigue, nocturia and increased urine production. Also called primary hyperaldosteronism.
• Conn-Louis Carcinoma: An uncommon (but possible highly underdiagnosed) condition characterized by the excessive production of a hormone called aldosterone by the adrenal gland. The condition results from the presence of an adrenal carcinoma. The severity of the condition is variable with some patients simply suffering high blood pressure and no other symptoms. Due to the high degree of variation in presenting symptoms, the condition may be frequently underdiagnosed or misdiagnosed.
• Conor's disease: An infectious disease that is caused by Rickettsia conorii which is transmitted by the brown dog tick (Rhipicephalus sanguineus). The disease occurs predominantly in Mediterranean areas such as India and Africa. The onset of symptoms is usually sudden and the incubation period is usually between 6 and 10 days.
• Conorenal Syndrome: A rare inherited disorder characterized mainly by kidney failure, abnormal bone development (cone-shaped epiphyses), eye problems and ataxia.
• Conotruncal heart malformations: A rare group of heart defect involving the outflow tracts. Examples include truncus arteriosus, transposition of great arteries and tetralogy of Fallot. Obviously the symptoms will be determined by which specific defect is involved.
• Conradi-Huenermann Syndrome: A rare genetic disorder characterized by growth deficiency, short limbs, large skin pores, sparse hair and other abnormalities.
• Conradi-Hunermann syndrome: A rare genetic disorder characterized by growth deficiency, short limbs, large skin pores, sparse hair and other abnormalities.
• Constrictive pericarditis: Inflammation, swelling and thickening of the pericardium (fibrous sac surrounding the heart) which causes it to tighten around the heart and affect its function. The condition may be misdiagnosed as a heart attack and vice versa.
• Constrictive tuberculous pericarditis: Inflammation and swelling of the pericardium (fibrous sac surrounding the heart) that occurs as a complication of tuberculosis. The condition may be misdiagnosed as a heart attack and vice versa.
• Cope's syndrome: Cope's syndrome is a condition where the body is too alkaline and the blood contains too much calcium. It can be caused by drinking large quantities of milk or using too many alkaline antacid remedies. High vitamin D intake can make the condition worse. The people most at risk of this condition tend to be older people (especially women) who are taking calcium supplements as well as calcium carbonate containing remedies to treat dyspepsia. Severe cases can lead to impaired kidney function (Burnett's syndrome).
• Copperhead snake poisoning: The Copperhead snake is a poisonous snake found mainly in parts of North America. The toxicity of the poison varies among species but some species are extremely poisonous and readily result in death if the patient is not treated.
• Cor Triatriatum: A rare congenital malformation where the heart has three atria instead of the normal two due to the presence of a separating membrane.
• Cor biloculare: A rare birth defect where the heart has two chambers instead of the normal four. The severity of the condition is variable with some cases being asymptomatic during infancy and survival has occurred for several decades in some cases. The defect rarely occurs on its own and is usually associated with various other malformations such as inverted abdominal organ positions.
• Coral snake poisoning: The Coral snake is a usually brightly colored, poisonous snake found mainly in America and Africa. The toxicity amongst species is variable. They are considered a shy snake and bites are usually the result of deliberate handling. Coral snakes have to bite for long enough to release the toxin through the fangs so envenomation tends to be rarer than for other snakes who can strike and envenomate rapidly. The snake venom contains toxins which mainly affect the nerve systems. Children tend to suffer more severe symptoms due to their smaller body size.
• Cordyceps-induced lead poisoning: Cordyceps is a folk remedy by Chinese people to treat high blood pressure, bleeding problems and diabetes. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Coronaro-cardiac fistula: An abnormal opening between a heart artery and a heart chamber or great vessel. This rare defect is present at birth and often causes no problems or symptoms until adulthood. The severity of the condition is determined by the size and exact location of the defect.
• Coronary arteries - congenital malformation: Abnormal coronary arteries present at birth. The coronary artery may be misplaced or deformed and the severity of the defect will determine the type and seriousness of symptoms. Some malformations produce no clinical symptoms whereas others are life-threatening without prompt treatment.
• Corpus callosum agenesis - blepharophimosis - Robin sequence: A very rare syndrome characterized by abnormal brain development, various facial anomalies, heart defects and other symptoms.
• Corpus callosum, agenesis of, blepharophimosis Robin type: A very rare syndrome characterized by abnormal brain development, various facial anomalies, heart defects and other symptoms.
• Cortes-Lacassie syndrome: A rare syndrome characterized by nail, hair and teeth abnormalities, malformed hands and feet and seizures. The disorder has only been reported in one cause which resulted in death at 31 months
• Cortical blindness - mental retardation - polydactyly: A very rare syndrome characterized by mental retardation, extra fingers and vision loss.
• Corticobasal Degeneration: A rare progressive neurological disorder where parts of the brain deteriorate.
• Corticosteroid-induced hypertension: Corticosteroid-induced hypertension is high blood pressure caused by use of corticosteroids. Patients with an existing history of hypertension may suffer further blood pressure increases while taking corticosteroids. Severity of symptoms varies amongst patients depending on their susceptibility, underlying health and duration of corticosteroid therapy.
• Coumachlor rodenticide poisoning: Coumachlor is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Coumafuryl rodenticide poisoning: Coumafuryl is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Coumatetralyl rodenticide poisoning: Coumatetralyl is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Crack addiction: An uncontrollable desire to use crack on a regular basis. Chronic crack use can lead to dependency in as little as two weeks. Crack is a form of cocaine - powdered cocaine is heated with ammonia or sodium bicarbonate to make rocks of crack. Frequent use leads to an increased tolerance to the drug so higher and higher doses are required to achieve the desired euphoric feeling.
• Crane-Heise syndrome: A very rare fatal disorder characterized by numerous abnormalities.
• Craniorachischisis: A rare malformation characterized by skull and spinal bone defects which leaves the brain and the nerves in the spine exposed. The severity of the condition is variable and generally results in death before or soon after birth. Often other defects such as imperforate anus or hernia is also present.
• Creutzfeldt-Jakob Disease: A very rare degenerative brain disease that can be inherited, transmitted (eg in surgical transplants using infected tissue) or as a result of genetic mutations. The condition is fatal.
• Croup: A condition characterized by an acute partial obstruction of the upper airway on young children
• Cryptococcosis: A fungal infection caused by Cryptococcus neoformans which primarily affects the central nervous system and the lungs. People with weakened immune systems such as AIDS sufferers are generally more susceptible to this type of infection.
• Crystal meth addiction: An uncontrollable desire to use crystal meth on a regular basis. Crystal meth is a powerful stimulant used illegally for its effects. It is highly addictive and known by street names such as ice, speed, glass, crank and chalk. Frequent use leads to an increased tolerance to the drug so higher and higher doses are required to achieve the desired euphoric feeling.
• Cuban lily poisoning: The Cuban lily is very toxic bulbous herb. It has long thin leaves with sprays of white, blue or purple bell-shaped flowers. The plant originated in Africa, Europe and Asia. Skin contact can cause skin irritation and eating parts of the plant can result in death. The toxic chemical in the plant is called cardiac glycoside.
• Cushing's syndrome-induced hypertension: Cushing's syndrome-induced hypertension is high blood pressure caused by a condition caused Cushing's syndrome where the adrenal glands produce excessive amounts of cortisol.
• Cutaneous T-cell lymphoma: A malignancy of the T-cells which make up part of the body's immune system. The cancer is characterized by the excessive proliferation of T-cells which are a type of white blood cell. The degree of skin involvement is variable.
• Cutaneous mucormycosis: An infectious disease caused by fungus from the order Mucorales which is normally found in the soil and in decaying plant matter. Transmission is usually through the inhalation of spores. It is generally harmless to healthy individuals but can cause infection in patients who are immunocompromised or who have a serious chronic illness such as uncontrolled diabetes. Symptoms and severity can vary considerable depending on the part of the body the infection occurs in - gastrointestinal tract, skin, lungs, central nervous system, eye orbit and the paranasal sinuses. Cutaneous mucormycosis is very rare and involves infection of the skin.
• Cutaneous photosensitivity colitis, lethal: A very rare syndrome where extreme sun sensitivity of the skin is associated with difficult to treat diarrhea. Death often occurs during infancy.
• Cutaneous zygomycosis: An infectious disease caused by fungus from the orders Mucorales and Entomophthorales which are normally found in the soil and in decaying plant matter. The infection differs from mucormycosis which only involves the order Mucorales. Transmission is usually through the inhalation of spores. It is generally harmless to healthy individuals but can cause infection in patients who are immunocompromised or who have a serious chronic illness such as uncontrolled diabetes. Symptoms and severity can vary considerable depending on the part of the body the infection occurs in - gastrointestinal tract, skin, lungs, central nervous system, eye orbit and the paranasal sinuses. Cutaneous zygomycosis involves infection of the skin.
• Cutler Syndrome: A rare disorder characterized by multisystem disorders including muscle wasting, ataxia, epilepsy, anemia and kidney disease. The kidney disease is most likely present at birth.
• Cyanide poisoning: Excessive ingestion of cyanide.
• Cyclosporin - Teratogenic Agent: There is evidence to indicate that exposure to Cyclosporin (an immunosuppressant drug) during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
• Cyclosporine - Teratogenic Agent: There is evidence to indicate that exposure to Cyclosporine (an immunosuppressant drug) during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
• Cyclosporine-induced hypertension: Cyclosporine-induced hypertension is high blood pressure caused by taking cyclosporine. Patients with an existing history of hypertension may suffer further blood pressure increases while taking amphetamines and this can be serious. Severity of symptoms varies amongst patients depending on their susceptibility, underlying health and duration of cyclosporine use.
• Cystic hygroma, lethal - cleft palate: A very rare lethal syndrome characterized mainly by cysts that form in the lymphatic system as well as an opening in the palate (cleft palate).
• Cysticercosis: An infectious disease caused by the pork tapeworm Taenia solium. If the larvae are ingested then a mild or asymptomatic tapeworm infection occurs. However, ingested eggs pass into the bloodstream where they can then enter various tissues and form the cysts that characterize cysticercosis.
• Cystosarcoma phyllodes: An aggressive type of malignant breast cancer.
• Cytomegalovirus: A easily transmissible viral infection that is common but generally causes no symptoms except in infants and people with weakened immune systems.
• Czeizel syndrome: A rare lethal syndrome characterized by cleft palate, uterus abnormalities and omphalocele (protrusion of abdominal organs such as intestine through the navel).
• D'Acosta: A condition that occurs when an un-acclimatized person climbs to high altitudes.
• Daffodil poisoning: Daffodils contain a toxic chemical which can cause poisoning symptoms if ingested. The plant also has the potential to cause skin reactions in susceptible people. The daffodil bulb contains the highest concentration of toxins and accidental ingestion has occurred when the bulb has been mistaken for an onion bulb.
• Dandy-Walker variant: A less severe form of a brain malformation called Dandy-Walker. The brain malformation involves the development of a cyst which may interfere with the drainage of cerebrospinal fluid and lead to hydrocephalus. Many patients don't have symptoms until adulthood or remain asymptomatic but some may be severely affected.
• Daphne poisoning: Daphne is a shrub that contains a toxin called mezerein (skin irritant) in the bark as well as a toxin called daphnin. The bark, sap and berries are the most toxic parts of the plant. The plant is native to Europe and Asia but is also found in other parts of the world such as America. A single berry or leaf can cause symptoms and 2 or 3 can cause death in a child. About 12 berries or leaves can cause quite severe symptoms in adults.
• Darvocet overdose: Darvocet is a prescription drug mainly used to treat pain. Excessive doses of the drug can result in various symptoms and even death in severe cases.
• De Sanctis-Cacchione syndrome: A rare genetic ectodermal disorder characterized by sunlight sensitivity, skin atrophy and pigmentation and skin tumors as well asneurologic involvement.
• Deadly nightshade (Solanum dulcamara) poisoning: The deadly nightshade is a woody vine and is considered quite toxic. It is found in Europe, Asia, North Africa and North America. There are a number of species of nightshade with variable toxicity. The Solanum dulcamara is considered less toxic with about 200 berries needed to cause death.
• Deafness - Opticoacoustic nerve atrophy - dementia: A rare genetic disorder characterized by degeneration of the optic nerve (causing impaired vision), deafness due to nerve damage and dementia due to calcification of the central nervous system. Death usually results by about the age of 40 with extensive calcification of all parts of the nervous system.
• Death: The loss of life.
• Death Angel poisoning: The Death Angel is a poisonous white, long-stemmed mushroom found mainly in the US.
• Death, Sudden, Cardiac: A term used to describe sudden, unexpected death due to the loss of heart function. The failure of the heart may be preceded by various symptoms or may occur without any warning. Sudden heart death may be caused by a variety of conditions such as drug abuse, blood vessel abnormalities and electrical abnormalities.
• Decompression sickness: Condition from overly rapid decompression, especially when diving.
• Defective apolipoprotein B-100: A rare inherited condition where defective apolipoprotein B-100 impairs the metabolism of cholesterol and results in high blood cholesterol which in turn increases the risk of cardiovascular disease.
• Defective expression of HLA class 2: An inherited immunodeficiency disorder which reduces the body's ability to fight infection. Lack of treatment can result in infant death from infection.
• Dehydration: Loss and reduction in body water levels
• Del(1) (p36.2-p36.1): A very rare chromosomal disorder where a portion of the short arm (p36.2-p36.1) of chromosome one is missing. The type and severity of symptoms is variable.
• Del(1) (q12-q21.3): A very rare chromosomal disorder where a portion of the long arm (q12-q21.3) of chromosome one is missing.
• Del(1) (q32-q42): A very rare chromosomal disorder where a portion of the long arm (q32-q42) of chromosome one is missing. The patient died within a week of birth in the reported case.
• Deletion 10pter: A very rare syndrome caused by a chromosomal defect (10p terminal deletion) and can result in a variety of malformations that are similar to DiGeorge syndrome and velocardiofacial syndrome.
• Deletion 4p: A rare chromosomal disorder where part or all of the short arm (p) of chromosome 4 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
• Demerol overdose: Demerol is a prescription drug used to treat pain. Excessive doses of the drug can result in various symptoms and even death in severe cases.
• Demyelinating disorder: Any condition that is characterised by the destruction of the myelin sheaths of the nerves
• Dengue fever: An acute viral disease characterized by fever, rash and myalgia and caused by a flavivirus which is transmitted by mosquitoes.
• Dengue hemorrhagic fever: Severe complication of dengue
• Dennis-Fairhurst-Moore syndrome: A very rare lethal syndrome characterized mainly by dwarfism, characteristic facial features, small eyes and reduced hair.
• Dermatomyositis: A muscle disease characterized by chronic muscle inflammation resulting in progressive muscle weakness and a characteristic rash.
• Deshi Dewa-induced lead poisoning: Deshi Dewa is a folk remedy by Indian people as a fertility medicine. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Desmoid disease, hereditary: A rare inherited disorder characterized by the development of benign growths called desmoid tumors or fibromatoses. The growth usually occurs in the abdomen but can occur in the neck, chest, arms and legs. Symptoms vary depending on the size and location of the growths. Even thought the growths are benign the can cause localized damage and obstruction. The condition can stabilize or become progressively worse and ultimately lead to death. The tumors often develop after some sort of trauma such as abdominal surgery or childbirth.
• Desmoplastic cerebral astrocytoma of infancy: A rare type of brain tumor that occurs in infants. The tumor consists of cancerous astrocytes.
• Desmoplastic infantile ganglioma: A rare type of brain tumor that occurs in infants. The tumor may be slow-growing and benign or fast-growing and malignant.
• Desmoplastic small round cell tumor: A rare aggressive tumor that usually develops in soft tissue and tends to grow to a large size. It usually occurs in the abdomen but may also in other parts of the body such as abdominal organs, brain, testicles, ovaries, spinal cord and skull.
• Desmosterolosis: A rare condition characterized by abnormal cholesterol biosynthesis where one of the intermediate products of cholesterol synthesis (desmosterol) is deposited in the body (plasma and other tissues). The condition also involves variable congenital anomalies which can be lethal in some cases.
• Desquamative Interstitial Pneumonia: A relatively uncommon form of lung inflammation that has no apparent cause though the majority of patients have a history of smoking. Symptoms tend to develop over a period of six months to one and a half years.
• Devil's Snuff Box poisoning: Devil's Snuff Box is a type of mushroom which has an extremely ugly appearance. These mushrooms are very poisonous and can cause death if eaten.
• Devil's trumpet poisoning: The Devil's trumpet is a shrubby plant with purple stems and large white or yellow flowers. The fruit is covered by a spiny shell. The plant originated in china and is often used as an ornamental outdoor plant. The plant contains tropane alkaloids which can be poisonous if eaten in large quantities.
• Dexedrine overdose: Dexedrine is a prescription drug mainly used to treat attention deficit hyperactivity disorder and narcolepsy. Excessive doses of the drug can result in various symptoms and even death in severe cases.
• Di Guglielmo I - chronic: A rare condition characterized by the presence of abnormal red blood cells in the bone marrow and blood. The condition is characterized by anemia and generally leads to the development of acute myelogenous leukemia. The chronic form has more severe symptoms than the acute form.
• DiGeorge syndrome: 22q11.2 deletion syndrome is a genetic disorder which can result in a vast array of symptoms. Various names have been used to describe different manifestations of the syndrome. Di George Syndrome primarily involves an underdeveloped thymus and parathyroid glands which results in lowered immunity low blood calcium levels respectively. Another primary feature is heart defects. Various other variable features are also present. It is not uncommon for patients to have more than one of the 22q11.2 deletion syndrome subtypes which can make diagnosis confusing - other subtypes include Sphrintzen syndrome, Caylor cardiofacial syndrome and CATCH 22.
• Diabetes-like symptoms: Symptoms similar to those of diabetes
• Dialysis encephalopathy syndrome: A progressive brain disease that occurs in some patients who undergo chronic hemodialysis. Aluminium intoxication is believed to play a role in the disease.
• Dialyzer hypersensitivity syndrome: An anaphylactic reaction that occurs in some patients who are dialyzed on artificial kidneys. A compound (ethylene oxide) used to dry sterilize artificial kidneys is a likely allergen.
• Diamond-Blackfan anemia: Diamond-Blackfan anemia is a rare genetic condition where the bone marrow is unable to make sufficient red blood cells which leads low levels of red blood cells. There are eight subtypes of the condition which differ in the location of the genetic defect and the incidence of additional symptoms such as malformations. The severity of symptoms is variable but most cases are serious.
• Diamond-Blackfan anemia 1: Diamond-Blackfan anemia is a rare genetic condition where the bone marrow is unable to make sufficient red blood cells which leads low levels of red blood cells. There are eight subtypes of the condition which differ in the location of the genetic defect and the incidence of additional symptoms such as malformations. Type 1 is caused by a defect on the RPS19 gene located on chromosome 18q13.2.
• Diamond-Blackfan anemia 2: Diamond-Blackfan anemia is a rare genetic condition where the bone marrow is unable to make sufficient red blood cells which leads low levels of red blood cells. There are eight subtypes of the condition which differ in the location of the genetic defect and the incidence of additional symptoms such as malformations. Type 2 is caused by a defect on chromosome 19q13.2.
• Diamond-Blackfan anemia 3: Diamond-Blackfan anemia is a rare genetic condition where the bone marrow is unable to make sufficient red blood cells which leads low levels of red blood cells. There are eight subtypes of the condition which differ in the location of the genetic defect and the incidence of additional symptoms such as malformations. Type 3 is caused by a defect on the RPS24 gene located on chromosome 10q22-q23.
• Diamond-Blackfan anemia 4: Diamond-Blackfan anemia is a rare genetic condition where the bone marrow is unable to make sufficient red blood cells which leads low levels of red blood cells. There are eight subtypes of the condition which differ in the location of the genetic defect and the incidence of additional symptoms such as malformations. Type 4 is caused by a defect on the RPS17 gene located on chromosome 15q.
• Diamond-Blackfan anemia 5: Diamond-Blackfan anemia is a rare genetic condition where the bone marrow is unable to make sufficient red blood cells which leads low levels of red blood cells. There are eight subtypes of the condition which differ in the location of the genetic defect and the incidence of additional symptoms such as malformations. Type 5 is caused by a defect on the RPL35A gene located on chromosome 3q29-qter.
• Diamond-Blackfan anemia 6: Diamond-Blackfan anemia is a rare genetic condition where the bone marrow is unable to make sufficient red blood cells which leads low levels of red blood cells. There are eight subtypes of the condition which differ in the location of the genetic defect and the incidence of additional symptoms such as malformations. Type 6 is caused by a defect on the RPL5 gene located on chromosome 1p22.1.
• Diamond-Blackfan anemia 7: Diamond-Blackfan anemia is a rare genetic condition where the bone marrow is unable to make sufficient red blood cells which leads low levels of red blood cells. There are eight subtypes of the condition which differ in the location of the genetic defect and the incidence of additional symptoms such as malformations. Type 7 is caused by a defect on the RPL11 gene located on chromosome 1p36.1-p35.
• Diamond-Blackfan anemia 8: Diamond-Blackfan anemia is a rare genetic condition where the bone marrow is unable to make sufficient red blood cells which leads low levels of red blood cells. There are eight subtypes of the condition which differ in the location of the genetic defect and the incidence of additional symptoms such as malformations. Type 8 is caused by a defect on the RPS7 gene on chromosome 2p25.
• Diaphanospondylodysostosis: A rare disorder characterized by bone formation anomalies including a lack of bone formation in the spine during the fetal stage as well as kidney problems.
• Diaphragm. congenital absence: A rare condition where an infant is born with part or all of the diaphragm missing. The diaphragm facilitates the breathing process and separates the abdominal organs from the chest organs.
• Diaphragmatic hernia - exomphalos - corpus callosum agenesis: A very rare syndrome characterized mainly by a diaphragmatic hernia (defect in the diaphragm that allows some of the abdominal organs to move into the chest cavity), brain development abnormalities and deafness.
• Diaphragmatic hernia, congenital: A birth defect involving an abnormal opening in the diaphragm which is a structure that assists breathing and keeps the abdominal organs from moving into the chest. The abdominal organs can protrude through this abnormal opening and restrict the growth of chest organs such as the lung and heart. The severity of the condition is variable depending on the size of the defect - some cases aren't diagnosed until adulthood.
• Diarrhea - polyendocrinopathy - infections, X-linked: A rare X-linked disorder characterized by diarrhea and severe, fatal infections during infancy. The body's immune system attacks it's own endocrine glands and various other organs. Females are carriers and can have mild symptoms whereas males suffer the fatal course of the disease.
• Diarrhea 2, with Microvillous Atrophy: A rare congenital condition characterized by diarrhea resulting form a defect in small intestine.
• Diastrophic dysplasia: A rare genetic disorder characterized by short stature as well as skeletal, spine and ear abnormalities.
• Difenacoum rodenticide poisoning: Difenacoum is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Difethialone rodenticide poisoning: Difethialone is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Diffuse neonatal hemangiomatosis: A very rare syndrome characterized mainly by multiple capillary hemangiomas as well as other abnormalities.
• Diffuse panbronchiolitis: A pulmonary disease involving chronic inflammation of the airways which causes obstruction and can lead to respiratory failure and even death if untreated.
• Digitalis - Teratogenic Agent: There is evidence to indicate that exposure to Digitalis (a heart drug) during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
• Digitorenocerebral syndrome: A very rare syndrome characterized by numerous abnormalities involving the brain, kidneys, fingers, toes, nails and face as well as mental retardation and vision impairment.
• Digoxin - Teratogenic Agent: There is evidence to indicate that exposure to Digoxin (a heart drug) during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
• Dilated cardiomyopathy: A rare chronic heart muscle condition where one or both heart ventricles are dilated or have impaired contractility.
• Dilated pupils: A condition characterized by the dilatation of the pupils of the eye
• Dilaudid overdose: Dilaudid is a prescription drug used mainly to treat pain. Excessive doses of the drug can result in various symptoms and even death in severe cases.
• Diphacinone rodenticide poisoning: Diphacinone is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Diphallus - rachischisis - imperforate anus: A very rare syndrome characterized mainly by genital abnormalities, absent anal opening and malformed vertebrae.
• Diphtheria: Infectious bacterial respiratory disease
• Disequilibrium syndrome: A complication that can occur during or after dialysis and probably caused by abnormal water balance within the brain. Swelling of the brain causes a range of neurological symptoms.
• Disseminated Vaccinia: Disseminated vaccinia is a serious complication of smallpox vaccination. The condition involves progressive death of tissue (necrosis) at the site of the vaccination. The condition is relatively rare but can result in death so prompt diagnosis and treatment is essential. People with AIDS, immunodeficiencies, cancer, receiving immunosuppressive therapies or have some other form of immune system defect are particularly susceptible to this complication.
• Dobriner syndrome: An inherited metabolic disorder involving a deficiency of coproporphyrinogen oxidase. The condition is similar to but milder than intermittent porphyria and sometimes includes photosensitivity.
• Double outlet right ventricle: A very rare birth defect where the aorta and the pulmonary artery both exit from the right ventricle and thus blood is unable to be pumped to the lungs. However, a hole connects the two ventricles and ultimately allows some blood flow to the lungs. The severity of symptoms varies depending on the location of the connecting hole in the heart and the exact location of the two arteries with respect to the heart.
• Doxepine-induced Immune Hemolytic Anemia: Doxepine -induced immune hemolytic anemia is a condition where use of a medication called Methyldopa triggers the body's immune system to destroy it's own red blood cells which results in anemia.
• Doxorubicin-induced cardiomyopathy: Heart disease caused by the use of a cancer drug called Doxorubicin.
• Drug Allergies: Allergies to medications or other drugs.
• Drug-induced Immune Hemolytic Anemia: Drug-induced immune hemolytic anemia is a condition where a medication triggers the body's immune system to destroy its own red blood cells which results in anemia. Certain drugs are more likely to trigger this abnormal immune response than others e.g. cephalosphorins and Quinidine.
• Drug-induced asthma: Drug-induced associated asthma refers to inflammation and constriction of the airways that is caused by taking a particular drug. There is a large range of drugs that have the potential to produce asthmatic symptoms in susceptible people. The severity of symptoms is variable.
• Drug-induced hypertension: Drug-induced hypertension is high blood pressure caused by taking certain drugs or medications e.g. corticosteroids, cyclosporine, amphetamines, alcohol and estrogens.
• Duchenne Muscular Dystrophy: An inherited degenerative disease of the muscles which progresses rapidly compared to other muscle wasting diseases.
• Duodenal atresia tetralogy of Fallot: A rare birth defect characterized by a heart defect and an intestinal malformation where the duodenum is absent or closed off which prevents digested material passing through.
• Dup (1)(pter-p31) and del(2)(q33-qter): A very rare chromosomal disorder where a portion of the short arm (pter-p31) of chromosome one is duplicated and a portion of the long arm (q33-qter) of chromosome 2 is deleted. The reported patient died at 3 months of age.
• Dup(1) (p31-p11): A very rare chromosomal disorder (one reported case) where a portion of the short arm (p31-p11) of chromosome one is duplicated. The type and severity of symptoms is variable.
• Dup(1) (p31-p21): A very rare chromosomal disorder where a portion of the short arm (p31-p21) of chromosome one is duplicated. The type and severity of symptoms is variable.
• Dup(1) (p34.1-p31): A very rare chromosomal disorder where a portion of the short arm (p34.1-p31) of chromosome one is duplicated.
• Dup(1) (p35-p31): A very rare chromosomal disorder where a portion of the short arm (p35-p31) of chromosome one is duplicated. The reported case resulted in death at 6 weeks of age.
• Dup(1) (q25-q32): A very rare chromosomal disorder where a portion of the long arm (q25-q32) of chromosome one is duplicated. The type and severity of symptoms may vary.
• Duplication 12q: A rare chromosomal disorder where there are three copies of the long arm (q) of chromosome 12 rather than the normal two resulting in various abnormalities. In most cases, death occurs during infancy. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is duplicated.
• Duplication 13: A rare and very severe chromosome disorder leading to mental retardation and physical defects. It is so severe that many babies die soon after birth. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is duplicated.
• Duplication 18: A rare genetic chromosomal syndrome where the child has an extra third copy of chromosome 18. Most fetuses are aborted before term, but a live birth with this condition occurs with a frequency around 1-in-3000. Duplication 18 syndrome is more severe than the more common Down syndrome. Duplication 18 syndrome causes mental retardation and numerous physical defects that often cause an early infant death. The condition has variable severity depending on how many of the body's cells have the extra chromosome and how much of the extra chromosome is duplicated. In severe forms all cells have an extra copy of the complete chromosome 18 whereas milder forms may have only some cells having the extra chromosome. Other mild forms may have an extra copy of only part of chromosome 18 in some or all of the body cells.
• Duplication 2q: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 2 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material.
• Duplication 7q: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 7 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material.
• Dwarfism lethal type advanced bone age: A rare lethal condition characterized by the association of dwarfism and advanced bone age.
• Dysbarism: A reaction caused by exposure to a sudden change in environmental pressure.
• Dysplastic cortical hyperostosis: A very rare syndrome characterized mainly by abnormal bone and brain development.
• Dyssegmental dysplasia: Any of a group of disorders characterized mainly by severe skeletal abnormalities. The type and severity of symptoms is variable as are the associated symptoms.
• Earthball poisoning: Earthball is a type of mushroom usually found in the US. The mushroom is very poisonous and can result in death if eaten.
• Eating symptoms: Symptoms related to eating.
• Ebola: Dangerous virus mostly found in Africa.
• Ebstein's anomaly: A heart defect where the tricuspid valve is malformed
• Eclampsia: serious complication of pregnancy and is characterised by high blood pressure and convulsions
• Ecstasy abuse: Use of the illicit drug called ecstasy
• Ecstasy addiction: An uncontrollable desire to use ecstasy on a regular basis. Chronic ecstasy use can lead to dependency in as little as two weeks. Ecstasy is a synthetic psychoactive drug often used as a recreational drug. Street names for the drug includes: XTC, Adam, Clarity, Lover's Speed, Hug, Beans and Love Drug. Frequent use leads to an increased tolerance to the drug so higher and higher doses are required to achieve the desired euphoric feeling.
• Ecstasy overdose: Ectsasy is an illegal and highly addictive recreational drug. Excessive doses of the drug can result in various symptoms and even death in severe cases.
• Ectodermal dysplasia, hypohidrotic, with immune deficiency: A rare genetic disorder characterized inability to sweat, immune system problems and hair and teeth abnormalities.
• Eczema vaccinatum: A rare condition where a person who has eczema and is exposed to vaccinia through vaccination. The condition can occur even if the inoculation doesn't occur directly onto eczematous skin. The virus can also be transferred to an eczema sufferer from a recently vaccinated person. Severe untreated cases can result in death.
• Edinburgh malformation syndrome: A rare syndrome characterized mental and physical retardation, infant death and various other abnormalities.
• Edward Syndrome: A rare genetic chromosomal syndrome where the child has an extra third copy of chromosome 18. Most fetuses are aborted before term, but a live birth with this condition occurs with a frequency around 1-in-3000. Duplication 18 syndrome is more severe than the more common Down syndrome. Duplication 18 syndrome causes mental retardation and numerous physical defects that often cause an early infant death. The condition has variable severity depending on how many of the body's cells have the extra chromosome and how much of the extra chromosome is duplicated. In severe forms all cells have an extra copy of the complete chromosome 18 whereas milder forms may have only some cells having the extra chromosome. Other mild forms may have an extra copy of only part of chromosome 18 in some or all of the body cells.
• Edwards Syndrome: A rare inherited genetic disorder where a portion of chromosome 18 is duplicated. Most affected individuals die during the fetal stage and surviving infants have serious defects and tend to live for only a short while.
• Ehlers Danlos syndrome type 4, autosomal dominant: A rare genetic connective tissue disorder characterized by delicate skin, fragile blood vessels, distinctive facial features and minimal joint problems - previously known as EDS type 4.
• Eijkman's syndrome: A group of nervous symptoms that is associated with vitamin B1 (thiamine) deficiency. The deficiency leads to a condition called Beri-Beri. Severe cases result in progressive paralysis leading to convulsions and death as the nerves become increasingly inflamed and wasted.
• Elapid poisoning: Sea snakes, Kraits and cobras are from the Elapid group of snakes. The toxicity of the venom varies depending on the species. The venom is usually toxic to the nerves or heart. Early symptoms such as drowsiness can occur within 30 minutes with more severe symptoms developing over the next few hours. Severe envenomation can result in death within hours.
• Electrical burns: Burns caused when an electric current pass through the body or part of it. The symptoms and severity of the burn depends on the strength of the electrical current, the duration of the exposure and the part of the body involved. Prompt treatment in more severe cases can improve the prognosis.
• Electrolyte abnormality: An imbalance in the level of any of a number of chemicals (electrolytes) in the blood stream e.g. chloride, sodium, magnesium, potassium, calcium, phosphate and bicarbonate. Symptoms can vary depending on which electrolyte is involved and the severity of the imbalance - severe cases can readily lead to death. An electrolyte abnormality can be caused by such things excessive loss of body fluid through vomiting or diarrhea, kidney conditions, malabsorption and various drugs such as diuretics and chemotherapy drugs.
• Elephant's-ear poisoning: The Elephant's ear is a common garden plant which has large, heart-shaped leaves on long stalks. The plant contains calcium oxalate and saphotoxin which can cause poisoning if eaten and irritation upon contact with skin or eyes. The toxins are quite poisonous and death can occur if sufficient quantities are eaten.
• Elliptocytosis 1: An inherited blood disorder where a significant number of red blood cells (erythrocytes) are elliptical or oval shaped rather than doughnut shaped. Anemia results when the abnormal red blood cells are destroyed. The severity of the anemia is variable with some cases resulting in fetal death and others being relatively asymptomatic. Type 1 is caused by a defect in the gene on chromosome 1p36.2-p34 for a protein in the red cell membrane.
• Ellis-Yale-Winter syndrome: A rare condition characterized by the association of a small head, congenital heart disease, lung segmentation defects and a missing kidney.
• Emerinopathy: A rare, progressive muscle disease that starts during childhood and involves muscle weakness and wasting.
• Encephalitis: Infection of the brain (as a symptom)
• Encephalopathy due to sulphite oxidase deficiency: An inborn error of metabolism where an enzyme (sulphite oxidase) deficiency results in encephalopathy. Symptoms usually start at birth.
• Endodermal sinus tumor: A form of malignant germ cell tumor that occurs mainly in young children. They can occur in the testis, ovaries, uterus, abdomen, thorax, tailbone region, vagina, liver, retroperitoneum and pineal ventricle of the brain. Symptoms will vary depending on the exact location of the tumor.
• Endometrial stromal sarcoma: A rare type of cancer that develops from the endometrial layer of the uterus. The cancer may be slow-growing or aggressive and may metastasize.
• Endomyocardial fibroelastosis: A rare heart malformation involving an abnormal thickening of the part of the heart muscle called the endocardium which affects the heart's function. Death is common in infancy and during early childhood.
• English Laurel poisoning: The English Laurel is an evergreen shrub with elongated spikes of flowers and white fruit with a black stone. The seeds, twigs and wilted leaves of the plant contain chemicals (cyanogenic glycoside, amygdalin) which are very poisonous and can cause death if eaten. The chemicals result in cyanide poisoning.
• Enteroaggregative E. Coli infection: A bacterial infection that results from ingesting contaminated food or water and results in diarrhea that tends to last for weeks. It most often causes diarrhea in children in developing countries. Enteroaggregative refers to the grouping nature of the bacterial attack on the intestinal lining.
• Enterohemorrhagic E. Coli infection: A bacterial infection that results from ingesting contaminated food or water and results in bloody diarrhea. Enterohemorrhagic refers to the intestinal bleeding associated with the infection.
• Enteropathogenic E. Coli infection: A bacterial infection that results from ingesting contaminated food or water and results in watery and sometimes bloody diarrhea. It most often causes diarrhea in infants in developing countries. Contaminated drinking water and meat products are the main source of infection. Enteropathogenic refers to the way that the bacteria use specific proteins to adhere to the intestinal lining.
• Enterotoxigenic E. Coli infection: A bacterial infection that results from ingesting contaminated food or water and results in diarrhea. It most often causes diarrhea in infants and travelers in underdeveloped countries where there is poor sanitation. Contaminated drinking water, soft cheese and raw vegetables are the main source of infection. Symptoms may vary from mild to severe. Enterotoxigenic refers to the fact that the bacteria produce toxins.
• Enterovirus antenatal infection: Fetal infection with enterovirus. The condition is extremely rare but infection around the time of birth often results in death or paralysis in survivors. The type and severity of symptoms is determined by the exact type of virus involved and at what stage of development the infection occurs.
• Envenomization by the Martinique lancehead viper: Posionous bite by a snake called the Lancehead Viper. It is a very venomous pit viper found in Martinique. Death is not common as the bite usually only causes a localized reaction rather than a systemic one. 10-20% of untreated cases result in death.
• Eosinophilic asthma: Eosinophilic asthma is a type of asthma that is characterized by increased levels of eosinophils (a type of white blood cell) in the airways. Asthma involves constriction and inflammation of the airways which makes breathing difficult. The severity of symptoms is variable.
• Ependymoma: A tumor that occurs in the central nervous system (brain and spinal cord). Symptoms vary according to the aggressiveness, size and exact location of the tumor.
• Epidemic typhus: An infectious disease caused by Rickettsia prowazekii and transmitted by body lice. The severity of the illness may range from moderate to fatal.
• Epidermolysa bullosa simplex and limb girdle muscular dystrophy: A rare syndrome involving fragile skin that blisters easily as well as muscle weakness and wasting in the head and limbs. The severity of the blistering and muscle weakness is variable with some sufferers dying during infancy.
• Epidermolysis bullosa: A group of rare inherited skin diseases characterized by fragile skin which forms blisters with even minor injuries. The blisters can be painful and can occur anywhere on the skin and even inside the digestive tract.
• Epidermolysis bullosa with pyloric atresia: A rare inherited blistering skin disorder which also involves a defect where the digestive system is closed off in the pyloric area. Death generally occurs even if the defect is corrected.
• Epidermolysis bullosa, junctional: A rare inherited skin disease which is characterized by fragile skin which readily forms skin blisters and can result in fatal complications.
• Epidermolysis bullosa, junctional, with pyloric atrophy: A rare inherited skin disease which is characterized by fragile skin which readily forms skin blisters as well as obstruction of the passage from the stomach to the intestine (pylorus). Death usually occurs within weeks of birth.
• Epidermolysis bullosa, lethal acantholytic: A very rare inherited disorder characterized by extremely fragile skin and mucous membranes which blisters and peels. The majority of the skin blisters and peels within a week of birth. Severe fluid loss and death follows soon after.
• Epiglotitis: Inflamation of the epiglottis in the throat
• Epilepsy: Paroxysmal transient disturbances of brain function that may manifest as loss of consciousness, abnormal motor phenomena
• Epileptic encephalopathy, early infantile, 1: A genetic form of epilepsy which is severe and starts during infancy. This form of the condition is caused by a defect on the ARX gene.
• Epiphyseal stippling syndrome - osteoclastic hyperplasia: A rare syndrome characterized by abnormal bone development primarily affecting the long bones and lower spine.
• Epithelial-myoepithelial carcinoma: A rare slow-growing type of cancer that occurs in the salivary duct - usually the parotid gland. The cancer tends to occur in older patients. The cancer tends to reoccur readily and can metastasize.
• Erb-Goldflam: An inherited disorder characterized by a defect in the transmission of signals to the muscles which results in muscle weakness.
• Erythroderma lethal congenital: A rare disorder which results in death within a year of birth and involves skin and growth problems.
• Erythrodermic eczema: Erythrodermic eczema is a severe condition that results from worsening eczema.
• Erythropoietin-induced hypertension: Erythropoietin-induced hypertension is high blood pressure caused by taking erythropoietin which is sometimes used to treat anemia in conditions such as chornic kidney failure. Patients with an existing history of hypertension may suffer further blood pressure increases while taking amphetamines and this can be serious. Severity of symptoms varies amongst patients depending on their susceptibility, underlying health and duration of erythropoietin use.
• Escharonodulaire: An infectious disease that is caused by Rickettsia conorii which is transmitted by the brown dog tick (Rhipicephalus sanguineus). The disease occurs predominantly in Mediterranean areas such as India and Africa. The onset of symptoms is usually sudden and the incubation period is usually between 6 and 10 days.
• Esophageal varices: Abnormally dilated blood vessels in the wall of the esophagus. The condition is asymptomatic unless the blood vessel bursts which can result in death.
• Esophagus symptoms: Symptoms affecting the esophagus (digestive throat passage)
• Esthesioneuroblastoma: A rare type of tumor that occurs in the upper nasal cavity. The tumor may obstruct one or both nostrils.
• Ewing's family of tumors: A rare condition where tumors develop in bone or soft tissue. Usually teenagers are affected.
• Exencephaly: A rare, fatal birth defect where parts of the skull bones are missing causing the brain to protrude.
• Exercise induced asthma: Exercise-induced asthma is a condition of respiratory difficulty that is triggered by aerobic exercise and lasts several minutes. Symptoms of EIA may resemble those of allergic asthma, or they may be much more vague and go unrecognized, resulting in probable underreporting of the disease.
• Exercise-induced anaphylaxis: Exercise-induced anaphylaxis is a syndrome in which patients experience the symptoms of anaphylaxis, which occur only after increased physical activity. The symptoms include pruritus and urticaria (typically with giant hives), and, without emergency intervention, the patient may develop hypotension and collapse.
• Extradural hematoma: Bleeding in the skull outside the brain
• Extragonadal Germ Cell Tumor: A rare form of cancer that originates in germ cells that are found in areas such as the brain, chest, tailbone or abdomen rather than the ovaries or testicles. Germ cells are the precursors for male sperm and female eggs. The symptoms are determined by the location and size of the tumor.
• Extranodal Marginal Zone B-cell Lymphoma of Mucosa-Associated Lymphoid Tissue: A rare type of cancer where the B cells (a type of white blood cell) in lymph tissue associated with mucosa begin to proliferate. The cancer can affect any mucosal membrane tissue but is most common in the gastric mucosal membranes. Symptoms may vary considerable depending on the stage and location of the cancer.
• Extrinsic asthma: Extrinsic asthma is a type of asthma that is triggered by an exposure to an allergen. Extrinsic asthma involves constriction and inflammation of the airways in response to exposure to the allergen. Examples of possible allergens include dust mites, pollen and mould. The severity of symptoms and allergen involved is variable.
• Eye defects - arachnodactyly - cardiopathy: A rare syndrome characterized mainly by eye defects, long, thin fingers and heart disease.
• FG syndrome 1: A rare inherited disorder characterized by anal abnormalities, reduced muscle tone and abnormal brain development. In type 1, the genetic defect is located on chromosome Xq12-q21.31.
• FG syndrome 2: A rare inherited disorder characterized by anal abnormalities, reduced muscle tone and abnormal brain development. In type 2, the genetic defect is located on chromosome Xq28.
• FG syndrome 3: A rare inherited disorder characterized by anal abnormalities, reduced muscle tone and abnormal brain development. In type 3, the genetic defect is located on chromosome Xp22.3.
• FG syndrome 4: A rare inherited disorder characterized by anal abnormalities, reduced muscle tone and abnormal brain development. In type 4, the genetic defect is located on chromosome Xp11.4-p11.3.
• FG syndrome 5: A rare inherited disorder characterized by anal abnormalities, reduced muscle tone and abnormal brain development. In type 5, the genetic defect is located on chromosome Xq22.3.
• Facies unusual arthrogryposis advanced skeletal malformations: A very rare fatal malformation characterized by an unusual facial appearance, arthrogryposis, advanced bone age of the hips and abnormal X-rays of the skeleton.
• Faciocardiorenal syndrome: A rare syndrome characterized by a variety of abnormalities such as kidney anomaly, mental retardation, unusual facial features, heart problems and joint problems. Infant death or stillbirth may occur in some cases.
• Fallopian tube cancer: A cancer that originates in the fallopian tubes which form part of the female reproductive organs. This type of cancer is relatively uncommon.
• False poinciana poisoning: False poinciana is a small tree with small leaves along divided branches. It has pea-like flowers and pods of fruit. The plant originated in South America. The seeds contain saponic glycosides and eating them can result in severe poisoning and even death if sufficient quantities are eaten. The plant is considered to be very poisonous.
• Familial Apolipoprotein A-I and C-III Deficiency: Familial Apolipoprotein A-I and C-III Deficiency is a lipid metabolism disorder characterized by low HDL cholesterol and a lack of apolipoproteins A-I and C-III in the blood.
• Familial Apolipoprotein A-I, C-III, A-IV Deficiency: Familial Apolipoprotein A-I, C-III and A-IV Deficiency is a lipid metabolism disorder characterized by low HDL cholesterol and a lack of apolipoproteins A-I and C-III in the blood.
• Familial Hypercholesterolemia: A genetic abnormality which causes patients to have abnormally high cholesterol levels (low-density lipoproteins). The condition usually leads to early cardiovascular disease.
• Familial Wilms tumor 2: A familial form malignant kidney tumor that occurs in children. Type 2 differs from other forms of Wilms tumor by the origin of the genetic defect (chromosome 19q13.4).
• Familial atrial fibrillation: A rare inherited condition where abnormal electrical activity in the heart causes it to have a fast and irregular beat. The condition may go unnoticed or may cause stroke or sudden death in some cases.
• Familial dilated cardiomyopathy: A rare inherited heart muscle condition where one or both heart ventricles are dilated or have impaired contractility. The heart becomes unable to pump sufficient blood around the body.
• Familial hyperlipoproteinemia: A group of genetic disorder characterized by abnormal breakdown of lipoproteins which causes abnormal lipoprotein and lipid levels in the blood. There are various types of this condition: hyperlipoproteinemia type I, II, III, IV and V. The type and severity of symptoms vary between types. The disorder tends to run in families (familial).
• Familial hypertrophic cardiomyopathy 1: An inherited condition characterized by increased thickness of the wall of the heart ventricle which affects the hearts function. Type 1 is caused by a defect on chromosome 14q12.
• Familial hypertrophic cardiomyopathy 10: An inherited condition characterized by increased thickness of the wall of the heart ventricle which affects the hearts function. Type 10 is caused by a defect in the MYL2 gene on chromosome 12q23-q24.
• Familial hypertrophic cardiomyopathy 11: An inherited heart condition involving thickening of the walls of the heart chambers which reduces the size of the heart chambers which restricts the outflow of blood from the heart ventricle and results in heart muscle disease. The condition may not cause any symptoms and can result in sudden death. Type 11 is caused by a defect in the ACTC1 gene on chromosome 15q14.
• Familial hypertrophic cardiomyopathy 12: An inherited heart condition involving thickening of the walls of the heart chambers which reduces the size of the heart chambers which restricts the outflow of blood from the heart ventricle and results in heart muscle disease. The condition may not cause any symptoms and can result in sudden death. Type 12 is caused by a defect in the CSRP3 gene on chromosome 11p15.1.
• Familial hypertrophic cardiomyopathy 2: An inherited condition characterized by increased thickness of the wall of the heart ventricle which affects the hearts function. Type 2 is caused by a defect in the troponin-T2 gene on chromosome 1q.
• Familial hypertrophic cardiomyopathy 3: An inherited condition characterized by increased thickness of the wall of the heart ventricle which affects the hearts function. Type 3 is caused by a defect in the alpha-tropomyosin gene on chromosome 15q22.1.
• Familial hypertrophic cardiomyopathy 4: An inherited condition characterized by increased thickness of the wall of the heart ventricle which affects the hearts function. Type 4 is caused by a defect in the cardiac myosin binding protein-C gene on chromosome 11p11.2.
• Familial hypertrophic cardiomyopathy 6: An inherited condition characterized by increased thickness of the wall of the heart ventricle which affects the hearts function. Type 6 is caused by a defect on chromosome 7q31-qter.
• Familial hypertrophic cardiomyopathy 7: An inherited condition characterized by increased thickness of the wall of the heart ventricle which affects the hearts function. Type 7 is caused by a defect in the TNNI3 gene on chromosome 19q13.4.
• Familial hypertrophic cardiomyopathy 8: An inherited condition characterized by increased thickness of the wall of the heart ventricle which affects the hearts function. Type 8 is caused by a defect in the MYL3 gene on chromosome 3p.
• Familial hypertrophic cardiomyopathy 9: An inherited condition characterized by increased thickness of the wall of the heart ventricle which affects the hearts function. Type 9 is caused by a defect in the TTN gene on chromosome 2q24.3.
• Familial infantile metachromatic leukodystrophy - late infantile: An infantile form of an inherited biochemical disorder involving a deficiency of an enzyme called cerebroside sulfatase. The enzyme deficiency causes cerebroside sulfate to build up within the body and causes damage to the nervous system including the brain. The late infantile form of this disease is much more common than the juvenile or adult form.
• Familial interstitial fibrosis: A rare familial disorder involving fibrosis and scarring of the lung tissue which causes the lung to become stiff and unable to function normally.
• Familial intestinal polyatresia syndrome: A rare birth malformation where the intestines are closed off or absent.
• Familial renal cell carcinoma: A genetic form of kidney cancer that develops in the lining of the tubules in the kidney and tends to run in families.
• Familial venous malformations: A rare condition where localized areas of blood vessels undergo changes and may result in bleeding. Severity of the condition depends on the location of these lesions. Lesions can occur in internal organs where bleeding can result in death. Lesions can also occur on the skin, inside the mouth and even on the genitals.
• Familial visceral myopathy: A rare condition where the duodenum is dilated and the muscles don't function normally which affects the movement of digestive waste material through the intestines. The symptoms of the condition are similar to that caused by an intestinal obstruction.
• Fanconi-ichthyosis-dysmorphism: A very rare syndrome characterized by scaly skin (ichthyosis), anemia, muscle anomalies and various other abnormalities. All six reported cases died within 6 months.
• Farber's disease: A rare inherited biochemical disorder involving the deficiency of an enzyme called ceramidase resulting in the harmful accumulation of certain chemicals in the body which causes damage and inflammation.
• Farouk-induced lead poisoning: Farouk is a folk remedy by Saudi Arabian people to treat teething. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Fazio-Londe syndrome: A rare inherited motor neuron disease characterized by progressive muscle weakness which ultimately leads to premature death.
• Febrile Ulceronecrotic Mucha-Habermann disease: A very rare skin disease characterized by bleeding skin ulcers and fever. There is no obvious cause of the condition. The skin ulcers spread and can cover most of the body. Sepsis and death is more likely in adults.
• Female pseudohermaphrodism - anorectal anomalies: A very rare disorder characterized by ambiguous external genitals and anal and rectal anomalies.
• Female sex reversal with dysgenesis of kidneys, adrenals and lungs: A very rare disorder involving female sex reversal and abnormal development of the lungs, kidneys and adrenals. Most of the reported cases were terminated during the fetal stage when the abnormalities were detected.
• Fetal Growth Retardation: Impaired growth of the fetus due to any cause. Causes include maternal cyanotic heart disease, chronic maternal hypertension, placental abnormalities and multiple births.
• Fetal akinesia syndrome, X-linked: A rare syndrome where the fetus is unable to move or has reduced mobility due to brain defects.
• Fetal aminopterin syndrome: A rare disorder which produces multiple abnormalities and results from a failed abortion attempt using the drugs aminopterin and methotrexate.
• Fetal and neonatal alloimmune thrombocytopenia: A rare, potentially life-threatening disorder where the mother's blood platelets are incompatible with that of the fetus and the mother's antibodies cross the placenta and destroy fetal platelets.
• Fetal death: The sudden unexpected death of a fetus
• Fetal indomethacin syndrome: Fetal exposure to indomethacin which is a nonsteroidal anti-inflammatory drug. The drug can pass through the placenta from the mother to the baby and cause various problems depending on what stage of development the fetus is at.
• Fetal parainfluenza virus type 3: Maternal infection with parainfluenza virus type 3 can cause a serious infection in the fetus and result in hydrocephalus. The risk is greatest during the first half of the pregnancy.
• Fetomaternal transfusion syndrome: A rare disorder where the blood from the fetus enters the mothers blood circulation through the placenta. This leads to anemia in the newborn. The passage of large amounts of blood from the fetus near the end of the pregnancy can result in serious consequences for the baby.
• Fetterbush poisoning: Fetterbush is an evergreen shrub which bears elongated spikes of small, urn-shaped flowers. The plant is found mainly in the US. The leaves and flower nectar contain andromedotoxin which is very poisonous if eaten. Severe poisoning can result in death.
• Fibrocartilaginous embolism: A rare disorder where some of the material from a vertebral disc enters the blood supply to the spinal cord where it causes an obstruction. Symptoms are determined by where the obstruction occurs. The obstruction causes damage to part of the spinal cord resulting in neurological symptoms which can result in death depending on the size and location of the obstruction.
• Filefish poisoning (Palytoxin): Palytoxin is a marine toxin found in some filefish from the Philippines and Singapore region. The toxin is extremely potent and death is common in patients who ingest contaminated filefish.
• Finale rodenticide poisoning: Finale is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Finnish lethal neonatal metabolic syndrome: A very rare lethal metabolic disorder characterized by a deficiency of complex III which causes brain, kidney and liver problems and ultimately results in early death.
• Fire Coral poisoning: The Fire Coral is a type of jellyfish with a seaweed-like appearance, found in warmer oceans around the world. The fire coral has stinging cells which can deliver a sting to humans. The fire coral has a hard skeletal portion which can also deliver cuts to the skin if it is brushed up against.
• Fire cherry poisoning: Fire cherry is a tree found mainly in the US. Ti bears round clusters of flowers and fruit with a large pit. The wilted leaves, stems and seeds contain cyanogenic glycoside and amygdalin which can be very poisonous if eaten. Severe cases of poisoning can result in death.
• Fixed pupils: stationary pupil unresponsive to all stimuli
• Flail chest: abnormal movement of a portion of the chest wall
• Flavivirus Infections: Infection with a virus from the Flaviviridae family of viruses. Infections by these pathogens include Dengue fever, Rocio encephalitis, West Nile virus and Japanese encephalitis. Transmission usually occurs through the bite of a mosquito.
• Flocoumafen rodenticide poisoning: Flocoumafen is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Florida leucothoe poisoning: The Florida leucothoe is a shrubby plant often grown in gardens. The leaves contain andromedotoxin which can cause serious symptoms if eaten. The plant is considered very poisonous and can result in death if sufficient quantities of leaves are consumed.
• Flu-like symptoms: Symptoms similar to flu including fever
• Fluoxetine - Teratogenic Agent: There is evidence to indicate that exposure to Fluoxetine during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
• Fluoxetine toxicity: The toxic reaction of the body to the substance, possibly via allergic reaction or overdose.
• Fluvoxamine toxicity: The toxic reaction of the body to the substance, possibly via allergic reaction or overdose.
• Foix-Alajouanine syndrome: A rare type of spinal cord disease caused by malformations in blood vessels supplying the spinal cord. Insufficient blood flow to the spinal cord causes muscle problems.
• Folgorat rodenticide poisoning: Folgorat is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Follicular dendritic cell tumor: A rare form of malignant tumor. Follicular dendritic cells are immune system cells found in lymph follicles. The tumor tends to be low grade and tends to reoccur after removal and occasionally metastasizes. The symptoms are determined by the location and size of the tumor. The tumor can occur on various parts of the body such as lymph nodes, tonsils, armpits and mediastinum but is most common in the neck lymph nodes.
• Follicular hamartoma - alopecia - cystic fibrosis: A rare syndrome characterized by small benign growths that develop in hair follicles, alopecia and cystic fibrosis.
• Food allergies: a food allergy is an adverse immune response to a food protein
• Food allergy related asthma: Food allergy related asthma refers to inflammation and constriction of the airways that is caused by an allergic reaction to a particular food. This is a very uncommon cause of asthma.
• Food poisoning: Poisoning from a substance or microbe in food.
• Fortaz - Teratogenic Agent: There is evidence to indicate that exposure to Fortaz (an antibiotic) during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
• Fowl Paralysis: A viral disease that affects poultry - it is very contagious and is a herpes virus. The virus tends to affect the nerves and cause tumors in internal organs. Poultry may be unable to lay eggs or may even die. Young birds are more susceptible than older birds with death most common between the ages of 8 and 20 weeks. The virus may attack the nervous system and result in paralysis or it may attack the visceral system and cause tumors in the internal organs. Some birds may die without any obvious symptoms.
• Fowl paralyses: A viral disease that affects poultry - it is very contagious and is a herpes virus. The virus tends to affect the nerves and cause tumors in internal organs. Poultry may be unable to lay eggs or may even die. Young birds are more susceptible than older birds with death most common between the ages of 8 and 20 weeks. The virus may attack the nervous system and result in paralysis or it may attack the visceral system and cause tumors in the internal organs. Some birds may die without any obvious symptoms.
• Foxglove poisoning: The foxglove is a herb which produces fruit in a capsule and colored, tubular flowers. The leaves, flowers and seeds of the plant contain a very toxic chemical called digitalis glycoside which can cause serious symptoms or even death if eaten. Skin irritation can occur if contact with the skin occurs. NOTE: Patients who are taking certain medications (digoxin, beta-blockers, calcium channel blockers) are more susceptible to foxglove poisoning.
• Fractures: Breakage of bones
• Francisella tularenis infection: Francisella tularenis is a type of bacteria that can cause infection involving the skin, respiratory and gastrointestinal systems. The nature and severity of symptoms varies depending on the location of the infection. The bacteria primarily causes localized tissue necrosis. The pathogen is considered a possible biological weapon.
• Franek-Bocker-Kahlen syndrome: A rare syndrome characterized mainly by a small head, brain defect, spasticity and high sodium level.
• Frank-Ter Haar syndrome: A rare genetic bone disorder characterized by skeletal abnormalities, enlarged corneas and characteristic facial abnormalities.
• Fraser-like syndrome: A very rare syndrome characterized by fused eyelids, airway anomalies, cysts in the ovaries and finger and toe abnormalities.
• Fried-Goldberg-Mundel syndrome: A rare syndrome characterized mainly by leg malformations and an abnormally positioned urethral opening (hypospadias) in males.
• Fructose-1-phosphate aldolase deficiency, hereditary: An inherited metabolic disorder where deficiency of the enzyme fructose-1-phsophate aldolase prevents fructose being metabolized resulting in fructose intolerance.
• Fryns Syndrome: A rare genetic disorder characterized by diaphragmatic abnormalities, coarse face and abnormal growth or development of ends of fingers and toes.
• Functioning pancreatic endocrine tumor: Tumors that develop in the pancreas and cause excessive secretion of one or more pancreatic hormones such as insulin, somatostatin, glucagons, gastrin, ACTH (corticosteroids) and vasoactive intestinal peptidase.
• Fungal meningitis: Fungal meningitis is an infection that causes swelling and irritation of the tissue around the brain and spinal cord. It usually strikes people whose weakened immune systems can't fight off infection. The disease is not common. but it can be very serious.
• Funnel Web spider poisoning: The funnel web spider is a poisonous spider found mainly in Australia and America. The venom is toxic to the nervous system. There are two phases of poisoning - the first phase starts soon after envenomation and may result in death in severe cases. The second phase occurs one or two hours after envenomation where patients may recover somewhat but symptoms such as apnea and low blood pressure may develop.
• GSD IIB - formerly: A rare inherited disorder characterized by severe heart problems, varying degrees of muscle weakness and often mental retardation. Other symptoms such as mental retardation may also occur. The genetic anomaly manifests as a deficiency of a protein called LAMP-2 (Lysosomal-Associated Membrane Protein 2) which affects lysosomes. The condition is now known as Danon disease.
• GSD2B - formerly: A rare inherited disorder characterized by severe heart problems, varying degrees of muscle weakness and often mental retardation. Other symptoms such as mental retardation may also occur. The genetic anomaly manifests as a deficiency of a protein called LAMP-2 (Lysosomal-Associated Membrane Protein 2) which affects lysosomes. The condition is now known as Danon disease.
• GSS (Gerstmann Sträussler Syndrome): Rare brain disease due to prions
• Ganglioglioma: A type of tumor that develops in the central nervous system. The tumor originates from glial and nerve cells. The tumor may grow rapidly and symptom will vary depending on the exact location and size of the tumor.
• Gangrene: Death (necrosis) of a portion of tissue or entire organ due to decreased perfusion with blood or infectious destruction of tissue.
• Garland flower Daphne poisoning: Garland flower Daphne is a small shrub bearing clusters of small pink or white fragrant flowers and white or yellow berries. The plant originated in Europe and is often used as an ornamental plant in gardens. The plant contains chemicals which can cause poisoning symptoms if eaten. Severe cases can result in death. Skin irritation can also occur on skin exposure.
• Gastro-enteropancreatic neuroendocrine tumor: A rare form of gastrointestinal tumor. It includes two main groups of cancer called carcinoid and endocrine pancreatic tumors. Some of the tumors consist of hormone secreting cells which results in excessive secretion of certain hormones.
• Gastrointestinal Stromal Tumors: Cancer that develops from stroma cells in the wall of the gastrointestinal tract. The primary locations are the small intestine, esophagus and esophagus with symptoms being determined by the location, stage and size of the tumor.
• Gastrointestinal bleeding: Bleeding in any part of the digestive tract
• Gastrointestinal mucormycosis: An infectious disease caused by fungus from the order Mucorales which is normally found in the soil and in decaying plant matter. Transmission is usually through the inhalation of spores. It is generally harmless to healthy individuals but can cause infection in patients who are immunocompromised or who have a serious chronic illness such as uncontrolled diabetes. Symptoms and severity can vary considerable depending on the part of the body the infection occurs in - gastrointestinal tract, skin, lungs, central nervous system, eye orbit and the paranasal sinuses. Gastrointestinal mucormycosis is very rare and involves infection of the gastrointestinal tract.
• Gastrointestinal neoplasm: A growth or excessive proliferation of cells in the lining of the gastrointestinal tract which includes the esophagus, intestine, pharynx and stomach. The growth may be benign or malignant. The symptoms are determined by the size, location and stage of the tumor.
• Gastrointestinal zygomycosis: An infectious disease caused by fungus from the orders Mucorales and Entomophthorales which are normally found in the soil and in decaying plant matter. The infection differs from mucormycosis which only involves the order Mucorales. Transmission is usually through the inhalation of spores. It is generally harmless to healthy individuals but can cause infection in patients who are immunocompromised or who have a serious chronic illness such as uncontrolled diabetes. Symptoms and severity can vary considerable depending on the part of the body the infection occurs in - gastrointestinal tract, skin, lungs, central nervous system, eye orbit and the paranasal sinuses. Gastrointestinal zygomycosis involves infection of the gastrointestinal tract.
• Gaucher disease - perinatal lethal form: A rare syndrome characterized by the association of abnormally tight skin and Gaucher disease which is a lipid storage disease. This is the most severe form of Gaucher disease.
• Gaucher ichthyosis restrictive dermopathy: A rare lethal condition characterized by the association of a lipid storage disease (Gaucher disease), congenital ichtyhosis and restrictive dermopathy.
• Gay-Feinmesser-Cohen syndrome: A very rare syndrome characterized mainly by short stature, congenital heart disease and an abnormal membrane of tissue across the larynx.
• Generalized pustular psoriasis: This is a rare form of psoriasis is also known as von Zumbusch psoriasis. It can be life-threatening especially in the elderly. It is characterized by the development of pustules in the flexural areas - the backs of the knees, the insides of the elbows, the armpits and the groin. These pustules continue to spread and soon they join to form lakes of pus. The pustules rupture easily and can become infected. This condition can be fatal if the patient gets dehydrated, or the infection spreads to the bloodstream. Generalized pustular psoriasis is often triggered by stopping topical or oral steroids.
• Generalized pustular psoriasis of pregnancy: A form of psoriasis that occurs during the third trimester of pregnancy and is characterized by pustules rather the skin bumps. The skin under and around the pustules is red and variable areas of skin may be involved. The pustules tends to occur in localized areas and then spreads to other parts of the body. It usually tends to recur during following pregnancies or with subsequent use of oral contraceptives.
• Genital herpes: Sexually transmitted infection of the genital region.
• Ghasard-induced lead poisoning: Ghasard is a lead-containing tetraoxide salt used mainly by Asian and Indian people as a tonic (usually for indigestion). This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Giant cell myocarditis: A rare cardiovascular disease involving inflammation of the heart muscle. The condition occurs for no apparent reason.
• Gila Lizard poisoning: Gila lizards are one of the few venomous species of lizard. They are found in parts of America such as Arizona, California, Nevada and Mexico. Envenomation by lizards is very uncommon but these venomous lizards can cause life-threatening symptoms. Gila lizards tend to hold on with their jaws while biting and the longer the jaws remain attached to the skin, the more severe the poisoning may be.
• Glanders: An infectious disease caused by a bacterium (Burkholderia mallei). It is usually a disease that affects horses and mules but can also infect other animals and humans. Human infection usually occurs in laboratory settings or in those with prolonged contact with infected animals. Symptoms are determined by whether infection occurs through the skin or via the lungs or blood stream. Bloodstream infections are the most severe and usually result in death within weeks.
• Glassy cell carcinoma of the cervix: A rare type of cervical cancer.
• Glioma: A rare type of tumor that occurs from glial cells that make up the central nervous system. These tumors usually occur in the brain but can also occur in the spinal cord and other nerves such as the optic nerve. Symptoms depend on the size and location of the tumor.
• Gliomatosis cerebri: A rare, aggressive type of malignant brain tumor. Cancerous glial cells infiltrate various parts of the brain and can result in a variety of symptoms.
• Gliosarcoma: A type of brain tumor that originates from glial cells. The tumor may grow rapidly and symptom will vary depending on the exact location and size of the tumor.
• Glory lily poisoning: The glory lily is a type of vine which bears unusual yellow and red flowers. It is often used as an indoor and outdoor ornamental plant. The plant contains various chemicals that can cause serious symptoms if eaten. The roots are the most toxic part of the plant. The plant is considered very toxic and serious cases can result in death.
• Glutamine deficiency, congenital: A rare genetic metabolic disorder characterized by a deficiency of the glutamine synthase enzyme. This results in a lack of glutamine in the serum, urine and brain and spinal fluid. The condition results in infant death within weeks of birth.
• Glutaric aciduria 2: A metabolic disorder involving an enzyme deficiency - electron transfer flavoprotein ubiquinone oxydoreductase. The severity of symptoms depends on the level of deficiency. The infant onset form is the most severe and often results in death. Severe cases usually develop during childhood or infancy and usually involve metabolic acidosis and its associated symptoms. Milder cases may simply present with muscle weakness initially that develops in adulthood. Some cases may involve additional symptoms such as heart, liver and kidney problems, facial anomalies and genital abnormalities.
• Glutaric aciduria type II: A rare disorder of amino acid metabolism characterized by a defect in the enzyme ETF (electron transfer flavenoid) or ETF dehydrogenase. The condition causes variable symptoms.
• Glutaricaciduria I: A rare inherited enzyme deficiency disorder where deficiency of the glutaryl-CoA dehydrogenase enzyme results in dystonia, dyskinesia and sometimes mental retardation.
• Glycine encephalopathy, classical neonatal early-onset form: A rare disorder of amino acid metabolism where glycine are unable to be metabolized properly due to defects in the glycine cleavage system. The early onset classical neonatal form usually starts after a period of normal development during the first 6 months of life.
• Glycine encephalopathy, classical neonatal form: A rare disorder of amino acid metabolism where glycine are unable to be metabolized properly due to defects in the glycine cleavage system.
• Glycine synthase deficiency: A rare genetic disorder characterized by high blood glycine levels which is toxic to the body. The severity of the condition varies according to the degree of deficiency and age of onset. The classical neonatal form is generally quite severe, the atypical mild form which generally includes symptoms such as aggressiveness, behavioral problems and speech problems. The transient neonatal form involves high blood glycine levels at birth which then returns to normal within a couple of months - there was no neurological or developmental impairment.
• Glycine synthase deficiency, type 1: A rare genetic disorder characterized by high blood glycine levels. It is caused by a defect in the P protein (pyridoxal phosphate-dependent glycine decarboxylase) in the energy creating center of cells (mitochondria).
• Glycine synthase deficiency, type 2: A rare genetic disorder characterized by high blood glycine levels. It is caused by a defect in the T protein (tetrahydrofolate-requiring enzyme) in the energy creating center of cells (mitochondria).
• Glycogen Storage Disease IIb - formerly: A rare inherited disorder characterized by severe heart problems, varying degrees of muscle weakness and often mental retardation. Other symptoms such as mental retardation may also occur. The genetic anomaly manifests as a deficiency of a protein called LAMP-2 (Lysosomal-Associated Membrane Protein 2) which affects lysosomes. The condition is now known as Danon disease.
• Glycogen storage disease type 2B: A rare inherited biochemical disorder involving the harmful accumulation of certain chemicals (glycogen) in body tissues due to the deficiency of an enzyme (?-glucosidase or acid maltase) needed to break it down. Type IIB usually starts during childhood.
• Glycogen storage disease type 2B - formerly: A rare inherited disorder characterized by severe heart problems, varying degrees of muscle weakness and often mental retardation. Other symptoms such as mental retardation may also occur. The genetic anomaly manifests as a deficiency of a protein called LAMP-2 (Lysosomal-Associated Membrane Protein 2) which affects lysosomes. The condition is now known as Danon disease.
• Glycogenosis type 2: A rare inherited biochemical disorder involving the harmful accumulation of certain chemicals (glycogen) in body tissues due to the deficiency of an enzyme (?-glucosidase or acid maltase) needed to break it down. The severity of the condition is variable and onset may occur during infancy, childhood or adulthood.
• Gnathostoma Infection: Infection with a type of round worm (Gnathostoma spinigerum and Gnathostoma hispidum). Infection typically occurs through eating undercooked fish or poultry containing the roundworm larvae or by drinking contaminated water. The symptoms are determined by which tissues the worms migrate through. The worms tend to migrate mainly through the skin.
• Goossens-Devriendt syndrome: A very rare syndrome characterized mainly by a brain defect, congenital heart disease and extra fingers.
• Granulomas, congenital cerebral: A rare birth condition characterized by granulomas in the brain. Cerebral granulomas are small inflamed areas of the brain. Death occurs with a day or so of birth.
• Granulomatous amebic encephalitis: Brain/CNS infection from Acanthamoeba bacteria
• Granulosa cell tumor of the ovary: A rare type of ovarian tumor which can cause excess estrogen hormone production. The tumor is a low grade malignant tumor.
• Graves disease: A condition which is an autoimmune disease that affects the thyroid resulting hyperthyroidism
• Gray baby syndrome: A side effect of chloramphenicol (antibiotic) administration to infants - especially premature infants. Infants lack the liver enzymes to metabolize the drug and it builds up to toxic levels. Death is relatively common.
• Grebe Syndrome: A rare genetic disorder characterized by very short limbs and extra fingers and toes.
• Green gill mushroom poisoning: Green gill is a type of mushroom with a smooth cap and white gills eventually turning greenish. The mushroom is commonly found growing naturally in the US. This mushroom is very poisonous and causes severe gastrointestinal symptoms. Severe poisoning can lead to death due to complications such as dehydration and electrolyte imbalance.
• Greenberg dysplasia: A very rare form of short-limbed dwarfism.
• Greenhead ant sting: The Greenhead ant is found in parts of Australia and can cause allergic reactions in susceptible people. Some people have a relatively minor allergic response whereas other develop anaphylaxis which is a life-threatening allergic response which requires urgent medical attention. The ants have a venom gland attached to a stinger located in their tail region. Ants can sting more than once.
• Greta-induced lead poisoning: Greta is a lead-containing tetraoxide salt used mainly by Mexican people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Griscelli disease: A rare genetic disorder characterized mainly by albinism (lack of pigmentation). There are three different subtypes of the disorder (I, II and III) each with varying additional features such as immunodeficiency and neurological symptoms. Type 1 involves partial albinism and neurological symptoms, type II involves partial albinism, immunodeficiency and sometimes neurological symptoms and type III involves albinism, only.
• Griscelli syndrome type II: A rare genetic condition characterized by a partial lack of pigmentation in the eye, skin and hair, clumps of pigmentation in hair shafts, immunodeficiency and neurological symptoms.
• Griscelli syndrome type III: A rare genetic condition characterized by a partial lack of pigmentation in the eye, skin and hair, clumps of pigmentation in hair shafts and immunodeficiency.
• Guam disease: A nerve degeneration disorder that occurs particularly in Guam and involves progressive dementia and parkinsonism which ultimately leads to death.
• Gustavson syndrome: A very rare condition characterized by features such as mental retardation, spasticity, seizures and eye and ear problems.
• HADH deficiency: A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activity prevents some fats being converted into energy. Symptoms tend to be exacerbated during fasting as during fasting, the body tries to rely more heavily on fats for energy. Fatty acids that are not completely metabolized due to the enzyme deficiency may build up in various organs and cause serious complications.
• HARD syndrome (Hydrocephalus - agyria - retinal dysplasia): A rare genetic disorder characterized by a smooth brain surface and eye, genitourinary and other abnormalities.
• HEC syndrome: A very rare syndrome characterized mainly by excess fluid inside the skull, cataracts and thickening of the heart.
• HELLP syndrome: A rare potentially fatal condition that occurs in pregnant women and is frequently associated with pre-eclampsia.
• HEM dysplasia: A rare disorder characterized by hydrops, dwarfism and abnormal bone calcification. The condition generally results in fetal death.
• HIV-1, CRF01_AE: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF A/E occurs mainly in Asia and originated in central Africa. It tends to be transmitted mainly through heterosexual contact i.e. infection occurs through mucosal exposure.
• HIV-1, CRF02_AG: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/G involves both And G subtypes. HIV-1, Group M, subtype CRF A/G occurs mainly in west and central Africas well as Taiwan.
• HIV-1, CRF04_ cpx: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/B involves both And B subtypes. HIV-1, Group M, subtype CRF_cpx is made up of a combination of subtypes A, G, H, K, and U - (cpx refers to a complex of two or more subtypes). This subtype has been diagnosed in Cyprus and Greece.
• HIV-1, CRF05_ D/F: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF D/F involves both D and F subtypes. HIV-1, Group M, subtype CRF D/F occurs mainly in the Democratic Republic of Congo.
• HIV-1, CRF06_cpx: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF06_cpx involves a combination of subtypes A, G, J and K - (cpx refers to a complex of two or more subtypes). This subtype has been diagnosed in Burkina Faso and Mali.
• HIV-1, CRF07_BC: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF07_BC involves a combination of type B' and C and is extremely rare.
• HIV-1, CRF08_BC: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF08_BC involves a combination of type B' and C and is extremely rare.
• HIV-1, CRF11_cpx: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF11_cpx is extremely rare and appears to include a mix of subtypes CRF01 (And E), A, G and J - (cpx refers to a complex of two or more subtypes).
• HIV-1, CRF12_BF: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF B/F has been diagnosed in Uruguay and Argentina.
• HIV-1, CRF13_cpx: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF13_cpx involves a combination of subtypes CRF01 (And E), A, G, J and U - (cpx refers to a complex of two or more subtypes).
• HIV-1, CRF14_BG: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF14_BG involves a combination of subtypes B and G. This subtype has been diagnosed in Spain.
• HIV-1, CRF15_01B: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF15_01B involves a combination of subtypes CRF01 (And E) and B.
• HIV-1, CRF16_ A2D: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF16_ A2D involves a combination of subtypes A2 and D. This subtype has been diagnosed in Kenyand South Korea.
• HIV-1, CRF17_BF: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF17_BF involves a combination of subtypes B and F.
• HIV-1, CRF18_cpx: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF18_cpx involves a combination of subtypes A, E, F, G, H, K and U - (cpx refers to a complex of two or more subtypes).
• HIV-1, CRF19_cpx: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF19_cpx involves a combination of subtypes A, E, D and G - (cpx refers to a complex of two or more subtypes).
• HIV-1, CRF20_BG: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF20_BG involves a combination of subtypes B and G. This subtype has been diagnosed in Cuba.
• HIV-1, CRF21_A2D: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF21_A2D involves a combination of subtypes A, D and G.
• HIV-1, CRF22_01A1: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF22_01A1 involves a combination of subtypes CRF01 (And E) and A1.
• HIV-1, CRF23_BG: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF23_BG involves a combination of subtypes B and G.
• HIV-1, CRF24_BG: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF24_BG involves a combination of subtypes B and G. This subtype has been diagnosed in Cuba.
• HIV-1, CRF25_cpx: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF25_cpx involves a combination of subtypes A, G and U - (cpx refers to a complex of two or more subtypes). This subtype has been diagnosed in Cameroon and Saudi Arabia.
• HIV-1, CRF26_AU: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF26_AU involves a combination of subtypes And U.
• HIV-1, CRF27_cpx: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF27_cpx involves a combination of subtypes A, E, G, H, J, K and U - (cpx refers to a complex of two or more subtypes). This subtype has been diagnosed in the Democratic Republic of Congo.
• HIV-1, CRF28_BF: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF28_BF involves a combination of subtypes B and F.
• HIV-1, CRF29_BF: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF29_BF involves a combination of subtypes B and F.
• HIV-1, CRF30_0206: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF30_0206 involves a combination of subtypes CRF02 (And G) and CRF06 (A, G, J and K).
• HIV-1, CRF31_BC: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF31_BC involves a combination of subtypes B and C.
• HIV-1, CRF32_06A1: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF32_06A1involves a combination of subtypes CRF06 (A, G, J, K) and A1.
• HIV-1, CRF33_01B: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF33_01B involves a combination of subtypes CRF01 (And E) and B. This subtype has been diagnosed in Malaysia.
• HIV-1, CRF34_01B: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF34_01B involves a combination of subtypes CRF01 (And E) and B. This subtype has been diagnosed in Thailand.
• HIV-1, CRF35_AD: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF35_AD involves a combination of subtypes And D. This subtype has been diagnosed in Afghanistan.
• HIV-1, CRF36_cpx: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF36_cpx involves a combination of subtypes CRF01 (And E), CRF02 (And G) and G - (cpx refers to a complex of two or more subtypes). This subtype has been diagnosed in Cameroon.
• HIV-1, CRF37_cpx: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF37_cpx involves a combination of subtypes CRF01 (And E), CRF02 (And G) and U - (cpx refers to a complex of two or more subtypes). This subtype has been diagnosed in Cameroon.
• HIV-1, CRF38_BF: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF38_BF involves a combination of subtypes B and F.
• HIV-1, CRF39_BF: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF39_BF involves a combination of subtypes B and F. This subtype has been diagnosed in Brazil.
• HIV-1, CRF40_BF: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF40_BF involves a combination of subtypes B and F. This subtype has been diagnosed in Brazil.
• HIV-1, CRF41_CD: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF41_CD involves a combination of subtypes C and D.
• HIV-1, CRF42_BF: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF42_BF involves a combination of subtypes B and F1.
• HIV-1, CRF43_02G: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype CRF43_02G involves a combination of subtypes CRF02 (And G) and G. This type has been diagnosed in Saudi Arabia.
• HIV-1A: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype A is most prevalent in West Africa.
• HIV-1A1: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. HIV-1A1 is a subtype of HIV-1A.
• HIV-1A2: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. HIV-1A2 is a subtype of HIV-1A.
• HIV-1A3: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. HIV-1A3 is a subtype of HIV-1A.
• HIV-1B: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype B is most prevalent in Thailand, Australia, Japan, Europe and America. This subtype tends to be transmitted mainly by homosexual contact and intravenous drug use i.e. infection occurs mainly through blood exposure.
• HIV-1C: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype C is most prevalent in Nepal, India and Southern and Eastern parts of Africa. This subtype tends to be a more virulent subtype and is transmitted mainly through heterosexual contact i.e. infection occurs through mucosal exposure.
• HIV-1D: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype D is most prevalent in the Eastern and Central parts of Africa and tends to be a more virulent subtype.
• HIV-1E: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype E has to date not occurred on its own but has occurred in combination with subtype A in a subtype called CRF A/E. This subtype occurs mainly in Asia and originated in central Africa. It tends to be transmitted mainly through heterosexual contact i.e. infection occurs through mucosal exposure.
• HIV-1F: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype F is most prevalent in Eastern Europe, South America and Central Africa.
• HIV-1F1: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. HIV-1F1 is a subtype of HIV-1F.
• HIV-1F2: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. HIV-1F2 is a subtype of HIV-1F.
• HIV-1G: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype G is most prevalent in Africa and central parts of Europe. This subtype tends to be a more virulent subtype.
• HIV-1H: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype H is most prevalent in central parts of Africa.
• HIV-1J: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype J is most prevalent in central America.
• HIV-1K: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group M, subtype K is most prevalent in the Democratic Republic of Congo and Cameroon.
• HIV-1M: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. HIV-1 group M is the most common form of HIV accounting for roughly 90% of cases worldwide.
• HIV-1N: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group N is very rare and has only been diagnosed in Cameroon.
• HIV-1O: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-1, Group O is very rare and has only been diagnosed in the western parts of Central Africa. This type is more difficult to diagnose and the standard test kits are not sensitive enough to pick up the virus.
• HIV-2: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. Group M is further classified into 9 subgroups - A to K and CRFs. CRF's are circulating recombinant forms which are a combination of any two subtypes e.g. CRF A/C involves both And C subtypes. HIV-2 is very rare and is generally only diagnosed in Africa but a number of cases have been diagnosed in the US. HIV-2 is less easily transmitted than HIV-1 and the time between infection and symptoms tends to be longer in HIV-2.
• HIV-2A: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. HIV-2 has two subtypes - And B and they are found mainly in Western Africa.
• HIV-2B: HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Once a person has been diagnosed with AIDS, even if treatment improved their CD4+ T cell count and infections are under control, the person is still considered to have AIDS. HIV is classified into two subtypes - HIV-1 and HIV-2. HIV-1 is further classified into three groups - Group M, N and O. HIV-2 has two subtypes - And B and they are found mainly in Western Africa.
• HMG-CoA lyase deficiency: A rare inherited metabolic disorder where deficiency of a particular enzyme impairs the processing of amino acids in food to create energy and causes various symptoms. Stresses on the body such as infection, fasting and heavy exercise can trigger an episode.
• Hai Ge Fen-induced lead poisoning: Hai Ge Fen is clamshell powder used mainly by Chinese people to make traditional Chinese herbal medicines. This product has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Hamman-Rich syndrome: A rare acute lung disease where the lung sufferers progressive inflammation and fibrosis which often leads to death.
• Hantavirosis: Infection by hantavirus which is a virus from the family Bunyaviridae. Infection generally causes severe febrile illness which can involve bleeding, shock and even death in some cases. The disease is transmitted by infected rodents.
• Hard skin syndrome, Parana type: A rare skin disorder characterized by rigid, thick skin that covers the whole body and affects movement. Tightness of skin over the chest and abdomen can impair breathing and death can result.
• Havoc rodenticide poisoning: Havoc is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Head injury: Any injury that occurs to the head
• Heart attack: An acute myocardial infarction
• Heart block progressive, familial: A rare degenerative disorder of the heart conduction system.
• Heart defects - limb shortening: A very rare syndrome characterized mainly by short limbs and heart defects.
• Heart failure: A condition which is characterized by an inability of the heart to pump blood efficiently and effectively
• Heart symptoms: Symptoms affecting the heart
• Heat stroke: it is a life threatening condition. It is hyperthermia in an advanced state
• Hemangioendothelioma: A rare type of blood vessel tumor that can occur anywhere in the body but is most often found in the skin, liver and spleen. Symptoms vary according to the exact location.
• Hemimegalencephaly: A very rare disorder where one side of the brain is bigger than the other.
• Hemoglobinopathy: A disease of the blood characterized by abnormal hemoglobin in the blood. The abnormality usually arises from a genetic defect which results in the hemoglobin have an abnormal structure. Sickle-cell disease and thalassemia are examples of hemoglobinopathies. Symptoms may vary from unnoticeable to severe with anemia being the most common symptom.
• Hemolytic uremic syndrome: A rare condition characterized by acute kidney failure, hemolytic anemia and thrombocytopenia (reduced blood platelet count). The condition is often caused by upper respiratory infections or infectious diarrhea.
• Hemolytic uremic syndrome, atypical, childhood: A rare disorder involving destruction of blood cells and kidney disease. Unlike typical hemolytic uremic syndrome which usually follows a bacterial infection, the atypical form is possibly a genetic disorder. The distinguishing feature of the atypical form is that no diarrhea is involved. The atypical form has a poorer prognosis than the typical form.
• Hemophagocytic lymphohistiocytosis, familial, 1: A rare recessively inherited disorder involving an overactive immune system. More specifically, the body becomes infiltrated by large numbers of histiocytes (macrophages) that accumulate in various organs such as the liver, spleen, bone marrow, skin and central nervous system. It usually only occurs in infants and young children and can be life-threatening.
• Hemophagocytic lymphohistiocytosis, familial, 2: A rare recessively inherited disorder involving an overactive immune system. More specifically, the body becomes infiltrated by large numbers of histiocytes (macrophages) that accumulate in various organs such as the liver, spleen, bone marrow, skin and central nervous system. It usually only occurs in infants and young children. Type 2 is caused by a defect on chromosome 10q22.
• Hemophagocytic lymphohistiocytosis, familial, 3: A rare recessively inherited disorder involving an overactive immune system. More specifically, the body becomes infiltrated by large numbers of histiocytes (macrophages) that accumulate in various organs such as the liver, spleen, bone marrow, skin and central nervous system. It usually only occurs in infants and young children. Type 3 is caused by a defect on chromosome 17q25.1.
• Hemophagocytic lymphohistiocytosis, familial, 4: A rare recessively inherited disorder involving an overactive immune system. More specifically, the body becomes infiltrated by large numbers of histiocytes (macrophages) that accumulate in various organs such as the liver, spleen, bone marrow, skin and central nervous system. It usually only occurs in infants and young children. Type 4 is caused by a defect on chromosome 6q24.
• Hemophagocytic reticulosis: The abnormal proliferation of reticulum cell (histiocytes) which infiltrate various organs and. Macrophages destroy blood cells causing blood abnormalities. Meningoencephalitis frequently occurs when the histiocytes infiltrate the mininges and cerebral tissue. Symptoms start at birth or soon after and become progressively worse without treatment. Medication can control the condition but a hematopoietic stem cell transplant is needed to achieve remission.
• Hemophilus influenzae B: Bacterial respiratory infection with dangerous complications.
• Hemorragic fever with renal syndrome: A group of infectious diseases that involve bleeding, fever and kidney problems. Examples of viruses that can cause such infectious diseases include Hantan virus, Puumala virus and Seoul virus. Examples of diseases caused by viruses in this group includes epidemic nephritis, Hantaan fever and Songo fever. The virus is usually transmitted to human by rodents or biting insects such as mosquitos. The severity and range of symptoms is determined by the particular virus involved.
• Hemosiderosis: A rare lung condition where bleeding into the lungs causes lung damage due to the accumulation of iron. The severity of the condition is determined by the amount of bleeding.
• Henna-induced lead poisoning: Henna is used mainly by Middle Eastern people as a hair and skin dye. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Heparin-induced thrombocytopenia: A blood disorder triggered by the use of the drug called heparin which is an anticoagulant. The severity of the condition is variable.
• Hepatic Venoocclusive Disease with immunodeficiency: An inherited disorder characterized by the association of immunodeficiency and liver disease involving the blockage of small veins in the liver due to swelling and fibrosis.
• Hepatic cystic hamartoma: A cystic liver tumor.
• Hepatic encephalopathy syndrome: A rare syndrome involving the association of advanced liver disease and neurological problems.
• Hepatic veno-occlusive disease - immunodeficiency: A rare form of liver disease involving the blockage of veins in the liver due to thickening of the blood vessel walls as well as immunodeficiency. The disease may be caused by a variety of factors including bone marrow transplant and genetic defects.
• Hepatitis: Any inflammation of the liver
• Hepatocellular carcinoma (fibrolamellar variant): A rare form of liver cancer. The prognosis for this variant of hepatocellular cancer is better than for hepatocellular cancer.
• Hepatoma: Hepatocellular carcinoma (HCC) is a primary malignancy of the liver.
• Herbal Agent overdose - Autumn Crocus: Autumn crocus can be used as a herbal agent to treat gout and rheumatoid conditions. The herbal agent contains chemicals such as colchicine and the ingestion of excessive amounts of this can result in symptoms. Severe overdose can result in death and chronic ingestion can also cause harmful effects.
• Herbal Agent overdose - Cleistanthus Collinus: Cleistanthus collinus can be used as a herbal agent which is very toxic and has been used to commit suicide or murder. The herbal agent contains toxic chemicals such as dyphyllin, collinusin and glycosides.
• Herbal Agent overdose - Golden Seal: Golden seal can be used as a herbal agent to treat a variety of conditions - bleeding after birth, mucosal inflammation, constipation, hemorrhoids. The herbal agent contains chemicals (alkaloid hydrastine, berberine) which can cause various symptoms if excessive quantities are taken.
• Hereditary carnitine deficiency: An inherited deficiency of carnitine resulting primarily in muscle problems. Severe symptoms can be triggered by periods of illness or fasting.
• Hereditary methemoglobinemia, recessive, type II: A rare inherited blood disorder where the hemoglobin (the oxygen-carrying part of red blood cells) can't bind with oxygen which impairs the oxygen supply to parts of the body, especially during exertion when more oxygen is needed by the body. The type II form of Gibson syndrome is more severe than type I and is characterized by cyanosis as well as neurological problems, mental deficiency and various other anomalies. Type I has enzyme deficiency (cytochrome B5 reductase) only in the red blood cells whereas in Type II the enzyme deficiency occurs in other body cells as well as red blood cells.
• Hereditary nodular heterotopia: A rare inherited disorder where a part of the brain tissue is misplaced during development. More specifically, nodules of brain tissue is in various parts of the brain.
• Hereditary pancreatitis: A rare inherited condition involving recurring bouts of pancreatitis (inflammation of the pancreas) often leading to chronic pancreatitis due to scarring of the pancreas.
• Hermaphroditism: A very rare genetic disorder where a baby is born having both male and female internal sex organs.
• Hernia: General term for an organ protruding where it should not.
• Heroin dependence: The physical and psychological dependence to the recreational drug heroin
• Heroin overdose: Heroin is an illegal and highly addictive recreational drug. Excessive doses of the drug can result in various symptoms and even death in severe cases.
• Herpes, Neonatal: Neonatal herpes is the infection of a newborn with the herpes virus within the first six weeks of life. The virus may be transmitted from the mother to the baby while it is still in the uterus or during delivery. The risk of transmitting the virus is highest if genital herpes is contracted during the late stages of the pregnancy. A mother with long standing or recurring herpes infection usually has sufficient antibodies to the virus to prevent the infant becoming infected. Neonatal herpes can also be contracted when an infant comes into contact with an infected person e.g. being kissed by and adult with cold sores. A cesarean birth may be advised for mothers who have active genital lesions.
• Herpes, Neonatal - Central Nervous System Infection: Central nervous system herpes infection in neonates is a herpes infection of the central nervous system (brain, spinal cord) that develops in infants within the first six weeks of life. The virus may be transmitted from the mother to the baby while it is still in the uterus or during delivery. The risk of transmitting the virus is highest if genital herpes is contracted during the late stages of the pregnancy. A mother with long standing or recurring herpes infection usually has sufficient antibodies to the virus to prevent the infant becoming infected. Neonatal herpes can also be contracted when an infant comes into contact with an infected person e.g. being kissed by and adult with cold sores. A cesarean birth may be advised for mothers who have active genital lesions. Central nervous system infection will occur in nearly three quarters of infants with a herpes infection.
• Herpes, Neonatal - Disseminated: Disseminated neonatal herpes is a widespread infection of a newborn with the herpes virus within the first six weeks of life. The virus may be transmitted from the mother to the baby while it is still in the uterus or during delivery. The risk of transmitting the virus is highest if genital herpes is contracted during the late stages of the pregnancy. A mother with long standing or recurring herpes infection usually has sufficient antibodies to the virus to prevent the infant becoming infected. Neonatal herpes can also be contracted when an infant comes into contact with an infected person e.g. being kissed by and adult with cold sores. A cesarean birth may be advised for mothers who have active genital lesions. Brain infection will occur in over half of infants with the disseminated form.
• Herring poisoning (clupeotoxin): Some herrings contain toxins (Clupeotoxin) which can be poisonous to humans if eaten. Heat does not destroy the toxin and there is still uncertainty as to the origin of the toxin. The toxin appears to be present in higher concentrations in summer and is believed to be possible linked to the consumption of toxic food in its food web. The size and age of the herring does not appear to be related to the toxicity. The herrings are found in coastal waters off Africa and the Caribbean, Indian and Pacific Oceans.
• Herrmann-Opitz craniosynostosi: A very rare syndrome characterized mainly by mental retardation, skeletal abnormalities and an unusual facial appearance.
• Heterozygous Familial Hypercholesterolemia: Heterozygous Familial Hypercholesterolemia is an inherited condition involving abnormal lipid metabolism. Cholesterol levels tend to be with coronary artery disease usually developing before the age of 50. The heterozygous form of the condition is not as severe as the homozygous form of the disease.
• High altitude cerebral edema: Brain condition related to high altitude.
• High altitude pulmonary edema: Lung condition related to high altitude.
• High blood pressure: Excessive blood pressure.
• Hing Torack Dowston syndrome: A rare syndrome that results in death due to severe malformations. The condition is similar to branchio-oculo-facial syndrome as it involves eye, facial and branchial abnormalities.
• His bundle tachycardia: A rare severe type of abnormal heart rhythm that occurs in infants less than 6 months old. Untreated, the condition can lead to heart disease and even death.
• Histiocytosis, Non-Langerhans-Cell: A group of disorders involving the excessive proliferation of histiocytes (macrophages) which are not Langerhans cells. Subgroups of this disorder includes hemophagocytic lymphohistiocytosis, sinus histiocytosis, xanthogranuloma and sea-blue histiocyte syndrome. Sometimes only the skin is involved and in other cases there may be systemic involvement which can cause serious problems.
• Hobo spider poisoning: The Hobo spider is a type of funnel web spider which can deliver a painful bite. Their bite can cause localized tissue necrosis which can take a long time to heal. Systemic symptoms may occur in severe cases but this is rare.
• Hodgkin disease, X-linked pseudoautosomal: An inherited form of Hodgkin disease which is a common cancer of the lymph node.
• Hoigné syndrome: Embolism (blood vessel blockage) and neurological problems associated with a procaine penicillin injection into the muscle. The condition is believed to be caused by some of the drug getting into the blood stream.
• Holoprosencephaly - caudal dysgenesis: A very rare syndrome where the tailbone and the portion above the tailbone (coccyx and sacrum) fail to develop. The brain also fails to divide into two lobes resulting in a single-lobed brain
• Holoprosencephaly - ectrodactyly - cleft lip/palate: A very rare syndrome characterized mainly by a cleft hand, lip and/or palate and the failure of the brain to separate into two lobes.
• Holoprosencephaly deletion 2p: A very rare syndrome characterized mainly by the failure of the brain to separate into two lobes, facial deformities and various other anomalies.
• Homicide: The killing of a person by another
• Homocystinuria: A rare inherited metabolic disorder involving the amino acid methionine and resulting in a harmful accumulation of homocysteine in the body.
• Homocystinuria due to cystathionine beta-synthase deficiency: A rare genetic biochemical disorder where a deficiency of cystathionine beta-synthase results in high levels of methionine and homocysteine in the blood and reduced levels of cyteine in the blood. There are two subtypes of the disorder with varying manifestations. One type responds to Vitmain B6 supplementation and the other doesn't. Those who do respond to Vitamin B6 tend to have milder manifestations.
• Homologous wasting disease: A term used to describe the disease state resulting from a graft versus host reaction. Graft versus host reaction occurs when the immune system of a transplant patient attacks the transplanted tissue but in homologous wasting disease the immune cells in the transplanted tissue actually attacks the host tissues. The condition occurs most often after a bone marrow transplant.
• Homozygous Familial Hypercholesterolemia: Homozygous Familial Hypercholesterolemia is a severe inherited condition involving abnormal lipid metabolism. Cholesterol levels tend to be very high with problems occurring early in life. Death from a heart attack can occur within the first few years of life in severe cases.
• Hookworm: Worm spread through feces with poor sanitation.
• Horse nettle poisoning: Horse nettle is a herbaceous plant which has prickles and bears yellow berries. The berries contain solanin alkaloids which can cause symptoms if eaten in large quantities. It is often found growing in the wild in many parts of the world. Death is considered possible if large amounts are eaten, especially in children.
• Horseshoe Crab poisoning: The Asiatic horseshoe crab is eaten mainly in parts of Asia. Various parts of the crab become toxic during the reproductive season - flesh, unlaid green eggs and viscera. Poisoning most often occurs in Thailand. Eating the crabs should be avoided during reproductive season as poisoning can readily result in death.
• Hoyeraal-Hreidarsson syndrome: A very rare syndrome characterized mainly by retarded growth, a small head, anemia, immunodeficiency and an underdeveloped brain (cerebellum).
• Human granulocytic ehrlichiosis: A rare infectious condition caused by infection with a type of bacteria called Ehrlichia (Anaplasma phagocytophilia) which attack granulocytes (a type of white blood cell). The infection is transmitted by the deer and American dog tick.
• Human monocytic ehrlichiosis: A rare infectious condition caused by infection with a type of bacteria called Ehrlichia (Ehrlichia chaffeensis) which attack monocytes(a type of white blood cell). The infection is transmitted by the Lone Star and American dog tick.
• Humerospinal dysostosis - congenital heart disease: A very rare syndrome characterized mainly by various skeletal defects and heart disease which is present at birth.
• Hyacinth bean poisoning: Hyacinth bean is a vine which bears elongated spikes of purple, white or pink flowers. The plant originated in Africa and is often used as an ornamental plant. The seeds and seed pod contain cyanogenic glycoside which can cause poisoning if large quantities are eaten. The seeds can be eaten if they are boiled for a long period of time with frequent water changes.
• Hyalinosis, infantile systemic: A rare genetic disorder involving abnormal deposits of hyaline throughout various body tissues. Manifestations include progressive joint contractures, skin abnormalities and pain.
• Hydatidosis: A parasitic infection caused by a tapeworm larva called echinococci. The type and severity of symptoms is determined by the location of the infestation - the most common site for the larval cysts is the liver. The most common symptoms are due to compression of nearby organs or blood vessels due to increasing size of the cyst. The larva may incubate for months or even years.
• Hydrocephalus: A condition which is characterized by marked dilatation of the cerebral ventricles
• Hydrocephaly corpus callosum agenesis diaphragmatic hernia: A very rare syndrome characterized mainly by a buildup of fluid inside the skull, abnormal brain development (corpus callosum) and a diaphragmatic hernia.
• Hydrocodone overdose: Hydrocodone is a prescription drug used mainly to treat pain. Excessive doses of the drug can result in various symptoms and even death in severe cases.
• Hydrops fetalis: Abnormal accumulation of fluid in the fetus which can be fatal. Excessive fluid leaves the blood and enters the tissues. It can have non-immune and immune (mother's immune system destroys fetal red blood cells).
• Hydroxyacyl-coa dehydrogenase, type 2, deficiency: A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Some cases simply involve developmental delay.
• Hyperaldosteronism-induced hypertension: Hyperaldosteronism -induced hypertension is high blood pressure caused by excessive production of a hormone called aldosterone by the adrenal glands. The high blood pressure often responds poorly to the usual medications. Death can result in severe cases.
• Hyperbilirubinemia transient, familial, neonatal: A rare inherited metabolic disorder where the body is unable to break down bilirubin which results in progressive jaundice which can be fatal or result in kernicterus (brain damage due to severe jaundice).
• Hyperdibasic aminoaciduria type 2: A rare inborn urea cycle disorder characterized by an enzyme defect in the amino acid transporter gene SLC7A7 (positive amino acid transporter).
• Hyperemesis Gravidarum: An extreme form of morning sickness.
• Hyperinsulinemic hypoglycemia, familial, 1: A disorder where too much insulin causes low blood sugar in infants. Prompt treatment is needed to avoid the brain being damaged by repeated periods of low blood sugar. The various types of familial hyperinsulinemic hypoglycemia are distinguished by their genetic origin. HHF1 is due to a mutation in the gene for SUR1 (surfonlyurea receptor 1) on chromosome 11p15.1.
• Hyperinsulinemic hypoglycemia, familial, 2: A disorder where too much insulin causes low blood sugar in infants. Prompt treatment is needed to avoid the brain being damaged by repeated periods of low blood sugar. The various types of familial hyperinsulinemic hypoglycemia are distinguished by their genetic origin. HHF2 is due to a mutation in the gene for Kir6.2 on chromosome 11p15.1.
• Hyperinsulinemic hypoglycemia, familial, 3: A disorder where too much insulin causes low blood sugar in infants. Prompt treatment is needed to avoid the brain being damaged by repeated periods of low blood sugar. The various types of familial hyperinsulinemic hypoglycemia are distinguished by their genetic origin. HHF3 is due to a mutation in the gene for glucokinase on chromosome 7p15-p13.
• Hyperinsulinemic hypoglycemia, familial, 4: A disorder where too much insulin causes low blood sugar in infants. Prompt treatment is needed to avoid the brain being damaged by repeated periods of low blood sugar. The various types of familial hyperinsulinemic hypoglycemia are distinguished by their genetic origin. HHF4 is due to a mutation in the gene for 3-hydroxyacyl-CoA dehydrogenase on chromosome 4q22-q26.
• Hyperinsulinemic hypoglycemia, familial, 5: A disorder where too much insulin causes low blood sugar in infants. Prompt treatment is needed to avoid the brain being damaged by repeated periods of low blood sugar. The various types of familial hyperinsulinemic hypoglycemia are distinguished by their genetic origin. HHF5 is due to a mutation in the insulin receptor gene on chromosome 19p13.2.
• Hyperinsulinemic hypoglycemia, familial, 6: A disorder where too much insulin causes low blood sugar in infants. Prompt treatment is needed to avoid the brain being damaged by repeated periods of low blood sugar. The various types of familial hyperinsulinemic hypoglycemia are distinguished by their genetic origin. HHF6 is due to a mutation in the GLUD1 gene on chromosome 10q23.3.
• Hyperlipoproteinemia: Hyperlipoproteinemia is a medical term for high levels of lipids in the blood which in turn causes high cholesterol levels. Lipoproteins are responsible for transporting cholesterol in the bloodstream and high levels of them in the bloodstream means that there are high levels of cholesterol in the bloodstream.
• Hyperlipoproteinemia type 3: A rare genetic disorder characterized by the body's impaired ability to break down certain lipids (triglycerides) which results in their buildup in the blood.
• Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome: A very rare inherited metabolic disorder where ammonia builds up in the body due to a defect in the transport of ornithine which prevents ammonia being converted to urea and being excreted through the urine. The severity of the condition is variable.
• Hyperoxia: A high level of oxygen in body tissues. It can be caused by exposure to high atmospheric pressure or long term inhalation of high oxygen concentrations. The high levels of oxygen may affect the lungs, nervous system or the eyes and thus can result in varying symptoms.
• Hypertelorism - esophageal abnormalities - hypospadias: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: one is inherited in a X-linked manner and the other is inherited in an autosomal dominant manner. Females with the X-linked form of the condition tend to have few symptoms and often only have wide set eyes.
• Hypertelorism with esophageal abnormality and hypospadias: A congenital disorder characterized by distinctive facial features, genital abnormalities, esophageal defect and difficulty swallowing. Males are more severely affected than females.
• Hypertension due to bilateral renal artery stenosis: Hypertension due to bilateral renal artery stenosis is high blood pressure resulting from narrowing kidney blood vessels which prevents the blood from flowing through the kidneys properly.
• Hypertension due to coarctation of the aorta: Hypertension due to coarctation of the aorta is high blood pressure resulting from a birth defect where a heart blood vessel called the aorta is abnormally narrowed. The high blood pressure tends to affect mainly the upper part of the body. Babies and very young children tend to have more severe symptoms as the degree of narrowing tends to be greater than in older children or adults.
• Hypertension of pregnancy: Pregnancy hypertension is the development of high blood pressure during pregnancy. Hypertension is a serious health condition due to the fact that it often causes no symptoms until it is severe. The increased blood pressure can cause complications in pregnancy women e.g. eclampsia and HELLP syndrome. The blood pressure usually returns to normal after delivery.
• Hypertrophic cardiomyopathy: Heart damage from thickened heart walls.
• Hypertrophic subaortic stenosis: A heart condition involving thickening of parts of the heart (usually the muscle wall separating the heart chambers) which reduces the size of the heart chambers (specifically the left ventricle). This abnormally thick heart muscle restricts the outflow of blood from the left heart ventricle and results in heart muscle disease. The condition is considered to be uncommon but not rare with as many as 1 in 500 people affected. The condition is usually caused by a genetic defect and the severity of the condition is variable.
• Hypoglycemia: Low blood sugar levels
• Hypokalemia: Abnormally low levels of potassium in the blood.
• Hypomandibular faciocranial dysostosis: A very rare syndrome characterized mainly by very underdeveloped upper and lower jaw as well as a very small, absent or small tongue.
• Hypoplastic thumbs - hydranencephaly: A very rare syndrome characterized mainly by underdeveloped thumb and abnormal brain development where the cerebral space is filled with cerebrospinal fluid instead of brain tissue.
• Hypospadias - hypertelorism: A congenital disorder characterized by distinctive facial features, genital abnormalities, esophageal defect and difficulty swallowing. Males are more severely affected than females.
• Hypothalamic hamartomas: A benign congenital tumor that develops on or near the hypothalamus.
• Hypothermia: Low body temperature
• Ichthyohepatotoxication: Ichthyohepatotoxication is a condition caused by eating the liver of certain fish. It is believed that the high vitamin A content of the liver leads to vitamin A overdose and the resulting symptoms. Tropical shark livers are associated with this condition.
• Ichthyosis - alopecia - eclabion - ectropion - mental retardation: A very rare syndrome characterized mainly by scaly skin, hair loss, mental retardation and outwardly turned eyelids and lips.
• Idiopathic basal ganglia calcification, childhood onset: A rare disorder involving the buildup of calcium deposits in various parts of the brain. It manifests as degeneration of the nervous system.
• Idiopathic dilation cardiomyopathy: A rare chronic heart muscle condition where one or both heart ventricles are dilated and the heart is unable to contract normally. In idiopathic forms, the condition occurs for no apparent reason.
• Idiopathic intestinal pseudoobstruction: A rare disorder where the patient suffers symptoms of an intestinal blockage but no such blockage is present. Malfunction of the muscle tissue of the intestines prevents normal movement of food through the digestive system and results in symptoms similar to that of a blockage.
• Idiopathic myopathy: A rare condition involving inflammation of the skeletal muscles which become weak and wasted.
• Idiopathic neonatal atrial flutter: A rare heart rhythm abnormality that occurs in neonates.
• Idiopathic, hypertrophic, subaortic stenosis: A rare heart disorder where thickening of parts of the heart (wall separating the heart chambers) reduces the size of heart chambers and hinders the flow of blood.
• Immunodeficiency, gonadal dysgenesis and pulmonary fibrosis: A rare syndrome characterized mainly by immunodeficiency, gonadal dysgenesis and pulmonary fibrosis that results in death.
• Immunosuppressive Measles Encephalitis: A rare complication of the measles virus. Some patients with a history of measles before the age of two develop progressive brain inflammation. The condition is rare and tends to only occur only in immunosuppressed children e.g. those who have acute lymphocytic leukemia. Symptoms may develop suddenly and tends to occur from weeks to months after the measles has resolved.
• Inborn amino acid metabolism disorder: A group of inherited disorders where the body is not able to metabolize amino acids consumed in the diet. Amino acids are a part of carbohydrates, fats and proteins and are metabolized in order to provide energy or to make other needed compounds. There are many steps involved in metabolism and the severity can be greatly variable depending on the exact nature of the disorder.
• Inborn urea cycle disorder: A genetic disorder involving a deficiency of one of the enzymes needed in the urea cycle. The urea cycle is the process of removing ammonia from blood stream by converting it to urea and excreting it via urine. A build-up of ammonia in the blood is toxic to the body and can cause serious brain damage. The progressively severe symptoms usually become obvious within the first few weeks of birth. Nevertheless, mild or partial enzyme deficiencies may cause little or no symptoms or symptoms that don't start until later in life.
• Inch ant sting: The Inch ant is found in parts of Australia and can cause allergic reactions in susceptible people. Some people have a relatively minor allergic response whereas other develop anaphylaxis which is a life-threatening allergic response which requires urgent medical attention. The ants have a venom gland attached to a stinger located in their tail region. Ants can sting more than once.
• Indandione rodenticide poisoning: Indandione is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• India tick typhus: An infectious disease that is caused by Rickettsia conorii which is transmitted by the brown dog tick (Rhipicephalus sanguineus). The disease occurs predominantly in Mediterranean areas such as India and Africa. The onset of symptoms is usually sudden and the incubation period is usually between 6 and 10 days.
• Indian Hemp poisoning: The Indian Hemp is a herbaceous shrubby plant who's sap contains resin and cardiac glycosides. Eating any part of the plant can result in cardiac arrest. The plant is considered very poisonous.
• Indian tick fever: An infectious disease that is caused by Rickettsia conorii which is transmitted by the brown dog tick (Rhipicephalus sanguineus). The disease occurs predominantly in Mediterranean areas such as India and Africa. The onset of symptoms is usually sudden and the incubation period is usually between 6 and 10 days.
• Infant asthma: Infant asthma is a type of asthma that occurs during childhood. Asthma involves constriction and inflammation of the airways. The severity of symptoms is variable. The asthma may be triggered by allergens, pollution, viral infections and many other factors.
• Infantile apnea: A disorder where infants stop breathing temporarily.
• Infantile sialic acid storage disorder: A rare inherited biochemical disorder characterized by the accumulation of sialic acid in the tissues and excretion of sialic acid in the urine. The disorder results in death within the first few years of life - usually in infancy.
• Inflammatory breast cancer: Inflammatory breast cancer is a rare and aggressive form of invasive breast cancer, where the skin of the breast becomes red, inflamed and pitted in appearance.
• Inhalant abuse: Inhalant abuse is the use of various inhalants for the purpose of achieving a "high". They are often used as a cheap, readily available alternative to street drugs but they can cause serious damage to the body. Inhalants include gasoline, adhesives, solvents, and aerosols. These inhalants can be abused by sniffing them, spraying directly into the mouth, heating them and then inhaling them or injecting them directly into the body.
• Inhalant addiction: Inhalant addiction refers to the compulsive need to abuse inhalants (e.g. inhaling them). Sufferers have withdrawal symptoms when attempting to stop the habit and feel unable to stop the habit despite knowing the harm it is causing their health. Inhalants are very damaging to the body and can readily result permanent brain damage and even death. Death can occur through chronic use and in rare cases can occur after one session of use. Children and teenagers are particular at risk for this type of addiction - it is readily available and users feel it gains them greater acceptance from their peers. Inhalants includes glues, shoe polish, household cleaners, room deodorizers and nail polish removers.
• Iniencephaly: A rare type of neural tube defect where the head is positioned in a backward bent angle and the spine is malformed.
• Insect allergy: An allergic response to a wasp sting.
• Insect bite allergy: An insect bite allergy is an adverse reaction by the body's immune system to a bite by an insect such as an ant. Multiple bites increase the risk of a severe reaction or death. The specific symptoms that can result can vary amongst patients.
• Insect sting allergies: When a person has an allergic reaction at the site of an insect sting
• Insect sting allergy: An insect sting allergy is an adverse reaction by the body's immune system to a sting by an insect such as an ant. Multiple stings increase the risk of a severe reaction or death. The specific symptoms that can result can vary amongst patients.
• Interferon Alpha - Teratogenic Agent: There is evidence to indicate that exposure to Interferon Alpha during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
• Intestinal capillariasis: Infection with a type of roundworm (Capillaria phillipinensis) found in the Phillipines and Thailand. Infection can occur by eating raw contaminated freshwater fish.
• Intestinal pseudoobstruction chronic idiopathic: A digestive disorder where the intestines are unable to contract normally and push food through the digestive system. This results in symptoms similar to an obstruction and hence the name pseudoobstruction. The condition has no obvious cause.
• Intracranial Embolism: Blockage of a blood vessel inside the skull and affects blood flow to parts of the brain. The severity of the condition is variable depending on the size, location and duration of the blockage.
• Intracranial Hemorrhages: Bleeding inside the skull. The condition is a medical emergency and the greater the bleeding, the more severe the condition.
• Intrahepatic cholangiocarcinoma: A slow growing malignant cancer that occurs in the bile ducts in the liver.
• Intrapartum Eclampsia: Intrapartum eclampsia is the development of seizures or coma in pregnant women suffering from high blood pressure. Intrapartum means that it occurs during the delivery of the baby. Eclampsia is a serious condition which requires urgent medical treatment. Eclampsia may be associated with moderate as well as significant increases in blood pressure. The blood pressure can return to normal after delivery or may persist for a period of time.
• Intrinsic asthma: Asthma that is not allergy related.
• Invasive candidiasis: Severe fungal infection usually in immunocompromised persons
• Irish potato poisoning: The common potato is an edible root. However, the potato sprouts and green skin in old potatoes contain chemicals such as solanine which can cause symptoms if eaten. Severe cases can result in death but this is relatively rare.
• Iron poisoning: Excessive ingestion of iron - often occurs when children ingest adult iron tablets.
• Isoniazid toxicity: The toxic reaction of the body to the substance, possibly via allergic reaction or overdose.
• Israeli spotted fever: An infectious disease that is caused by Rickettsia conorii which is transmitted by the brown dog tick (Rhipicephalus sanguineus). The disease occurs predominantly in Mediterranean areas such as India and Africa. The onset of symptoms is usually sudden and the incubation period is usually between 6 and 10 days.
• Isthmus coarctation: A rare inherited birth defect where the heart blood vessel called the aorta has a narrowed area which affects blood flow. The degree of constriction is variable which mild cases asymptomatic until adulthood. The poor blood flow to the lower body gives results in it appearing less developed than that upper body.
• Ivemark II: A lethal syndrome characterized by lack of spleen function as well as kidney, liver, pancreatic and heart abnormalities. The condition generally results in death within days of birth.
• Ives-Houston syndrome: A rare inherited syndrome characterized by retarded fetal growth, small head, malformed limbs and death before or soon after birth.
• Jack jumper ant sting: The jack jumper ant is commonly found in many parts of Australia and can cause allergic reactions in susceptible people. Some people have a relatively minor allergic response whereas other develop anaphylaxis which is a life-threatening allergic response which requires urgent medical attention. Jack jumpers deliver their venom by grabbing skin in its jaws and then using a stinger located in their tail region to inject the venom.
• Jamaican vomiting sickness: A fatal reaction to eating unripe ackee fruit.
• Japanese andromeda poisoning: An evergreen flowering shrub originating from Asia. The leaves and flower nectar contain a chemical called andromedotoxin which is highly toxic. Ingesting the leaves or nectar can result in death as the plant is considered highly toxic.
• Japanese encephalitis: A form of encephalitis caused by a flavivirus (Japanese B encephalitis virus - JBEV) and transmitted by mosquito bites. Most cases are mild and asymptomatic but severe cases can lead to death.
• Japanese skimmia poisoning: Japanese skimmia is a shrub which bears clusters of whitish, scented flowers on a purple-red stalk and bright red fruit. The plant originated in Japan and is often used as an ornamental plant in gardens. The plant, especially the red fruit, contains toxic chemicals which can cause serious heart problems if large quantities are eaten. Ingesting the fruit can also result in loss of fetus. The plant is only considered toxic if large quantities are eaten.
• Jensen syndrome: A rare genetic disorder characterized by degeneration of the optic nerve (causing impaired vision), deafness due to nerve damage and dementia due to calcification of the central nervous system. Death usually results by about the age of 40 with extensive calcification of all parts of the nervous system.
• Jervell and Lange-Nielsen Syndrome: A rare condition characterized by congenital deafness and a long Q-T interval which is where the heart takes longer than normal to recharge after a heartbeat.
• Jin Bu Huan-induced lead poisoning: Jin Bu Huan is a folk remedy used mainly by Chinese people to treat pain. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Jirásek-Zuelzer-Wilson syndrome: A rare abnormality that can occur in newborn infants and involves a complete lack of nerve tissue in the entire colon. The colon is unable to move digesting material through it and leads to a blockage of the digestive system.
• Johnson-Hall-Krous syndrome: A rare congenital disorder characterized by cataracts, cleft palate, high nose bridge, extra finger and tongue abnormalities.
• Johnston Aarons Schelley syndrome: A very rare lethal syndrome characterized mainly by contractures and thickened skin.
• Jonquil poisoning: The Jonquil is a pretty flowering bulb plant. The bulb contains phenanthridine alkaloids and calcium oxalate crystals which can cause symptoms if ingested. Generally, toxicity only occurs if large quantities are eaten. Severe skin irritation can occur upon skin contact.
• Jugular lymphatic obstruction sequence: A rare disorder caused by obstruction of the jugular lymphatic system due to problems during the fetal stage of development.
• Jumper syndrome: Injuries resulting from jumping or falling from a height.
• Juvenile Scleroderma: Scleroderma that occurs in children. Scleroderma is a connective tissue disease that can affect the skin, blood vessels, the immune system and sometimes even the organs may be involved. The disorder may be localized or affect large areas of the body.
• Juvenile gout: Gout that occurs in children as a result of kidney disease caused by a genetic defect.
• Kandu-induced lead poisoning: Kandu (red powder) is a folk remedy used mainly by Asian and Indian people to treat intestinal problems. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Kaplan-Plauchu-Fitch syndrome: A very rare syndrome characterized mainly by cone-shaped skull, short stature, deafness and various facial and digital abnormalities.
• Kennerknecht-Sorgo-Oberhoffer syndrome: A very rare syndrome characterized mainly by absent gonads and an underdeveloped right side of the heart.
• Kenny-Caffey syndrome, Type 1: A very rare inherited skeletal disorder involving thickening of the long bones of the body and head abnormalities. Type 1 is inherited in a recessive manner and is caused by a genetic defect located at chromosome 1q42-q43.
• Kenny-Caffey syndrome, Type 2: A very rare inherited skeletal disorder involving thickening of the long bones of the body and head abnormalities.
• Kenya fever: An infectious disease that is caused by Rickettsia conorii which is transmitted by the brown dog tick (Rhipicephalus sanguineus). The disease occurs predominantly in Mediterranean areas such as India and Africa. The onset of symptoms is usually sudden and the incubation period is usually between 6 and 10 days.
• Kenya tick typhus: An infectious disease that is caused by Rickettsia conorii which is transmitted by the brown dog tick (Rhipicephalus sanguineus). The disease occurs predominantly in Mediterranean areas such as India and Africa. The onset of symptoms is usually sudden and the incubation period is usually between 6 and 10 days.
• Kenya tick-bite fever: An infectious disease that is caused by Rickettsia conorii which is transmitted by the brown dog tick (Rhipicephalus sanguineus). The disease occurs predominantly in Mediterranean areas such as India and Africa. The onset of symptoms is usually sudden and the incubation period is usually between 6 and 10 days.
• Keratosis follicularis - dwarfism - cerebral atrophy: A very rare syndrome characterized mainly by dwarfism, brain degeneration and a hair follicle disorder.
• Keratosis palmoplantaris - adenocarcinoma of the colon: A rare disorder characterized by cancer of the secretory lining of the colon as well as thickening of the skin on the palms and soles. The colon cancer tends to grow slowly.
• Kernicterus: passage of bilirubin though the blood brain barrier
• Kidney damage - 1,2-Dichloromethane: Damage or injury to kidneys caused by exposure to a hydrocarbon called 1,2-Dichloromethane. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Acetaminophen: Damage or injury to kidneys caused by a type of analgesic called acetaminophen (Tylenol). Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Aminoglycosides: Damage or injury to kidneys caused by aminoglycoside antibiotics. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Aminosalicylic Acid: Damage or injury to kidneys caused by a type of antibiotic called aminosalicylic acid. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Amphotericin B: Damage or injury to kidneys caused by an antibiotic called amphotericin B. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Amyl Alcohol: Damage or injury to kidneys caused by exposure to amyl alcohol. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Anti-cancer drugs: Damage or injury to kidneys caused by exposure to anti-cancer drugs such as cyclosporine and cisplatin. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Aristolochic acid: Damage or injury to kidneys caused by exposure to aristolochic acid. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Arsenic: Damage or injury to kidneys caused by exposure to arsenic. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Aspirin: Damage or injury to kidneys caused by a type of analgesic called Aspirin. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Automobile exhaust: Damage or injury to kidneys caused by exposure to Automobile exhaust. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Bacitracin: Damage or injury to kidneys caused by a type of antibiotic called bacitracin. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Bismuth: Damage or injury to kidneys caused by exposure to bismuth. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Cadmium: Damage or injury to kidneys caused by exposure to cadmium. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Carbon Tetrachloride: Damage or injury to kidneys caused by exposure to Carbon tetrachloride. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Cephaloridine: Damage or injury to kidneys caused by a type of antibiotic called Cephaloridine. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Chloroform: Damage or injury to kidneys caused by exposure to a hydrocarbon called chloroform. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Chlorotetracycline: Damage or injury to kidneys caused by a type of antibiotic called Chlorotetracycline. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Chromium: Damage or injury to kidneys caused by exposure to chromium. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Cisplatin: Damage or injury to kidneys caused by exposure to an anti-cancer drug called Cisplatin. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Contrast agents: Damage or injury to kidneys caused by a contrast agent called sodium iodide used in some diagnostic tests. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Copper: Damage or injury to kidneys caused by exposure to copper. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Cyclophosphamide: Damage or injury to kidneys caused by exposure to an anti-cancer drug called Cyclophosphamide. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Cyclosporin: Damage or injury to kidneys caused by exposure to an anti-cancer drug called cyclosporine. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Degreasing solvents: Damage or injury to kidneys caused by exposure to degreasing solvents. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Dichloroacetylene: Damage or injury to kidneys caused by exposure to a hydrocarbon called Dichloroacetylene. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Diethylene glycol: Damage or injury to kidneys caused by exposure to a hydrocarbon called Diethylene glycol. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Dioxane: Damage or injury to kidneys caused by exposure to a hydrocarbon called Dioxane. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Ethylene Glycol: Damage or injury to kidneys caused by exposure to ethylene glycol. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Ethylene glycol ethers: Damage or injury to kidneys caused by exposure to Ethylene glycol ethers. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Fuels: Damage or injury to kidneys caused by exposure to fuel. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Gasoline: Damage or injury to kidneys caused by exposure to gasoline. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Germanium: Damage or injury to kidneys caused by exposure to germanium. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Glue solvent vapors: Damage or injury to kidneys caused by exposure to glue solvent vapors. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Glues: Damage or injury to kidneys caused by exposure to glues. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Gold: Damage or injury to kidneys caused by exposure to gold. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Hairdressing solvents: Damage or injury to kidneys caused by exposure to hairdressing solvents. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Hairdressing sprays: Damage or injury to kidneys caused by exposure to hairdressing sprays. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Heavy metals: Damage or injury to kidneys caused by exposure to heavy metals. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Herbicide: Damage or injury to kidneys caused by exposure to herbicides. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Hexachloro-1,3-butadiene: Damage or injury to kidneys caused by exposure to a hydrocarbon called Hexachloro-1,3-butadiene. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Hydrocarbons: Damage or injury to kidneys caused by exposure to hydrocarbons such as chloroform and styrene. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Ibuprofen: Damage or injury to kidneys caused by a type of analgesic called Ibuprofen. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Lead: Damage or injury to kidneys caused by exposure to lead. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Lithium: Damage or injury to kidneys caused by exposure to lithium. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Mercury: Damage or injury to kidneys caused by exposure to mercury. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Methanol: Damage or injury to kidneys caused by exposure to methanol. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Methemoglobin-producing agents: Damage or injury to kidneys caused by exposure to methemoglobin-producing agents. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Methicillin: Damage or injury to kidneys caused by a type of antibiotic called methicillin. Kidney damage usually occurs as a result of an allergic reaction to the antibiotic. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Neomycin: Damage or injury to kidneys caused by a type of antibiotic called Neomycin. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Nonsteroidal anti-inflammatory drugs: Damage or injury to kidneys caused by a type of analgesic called nonsteroidal anti-inflammatory drugs. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Oxytetracycline: Damage or injury to kidneys caused by a type of antibiotic called Oxytetracycline. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Paint solvents: Damage or injury to kidneys caused by exposure to paint solvents. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Paint thinners: Damage or injury to kidneys caused by exposure to paint thinners. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Paints: Damage or injury to kidneys caused by exposure to paints. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Paraquat ochratoxin A: Damage or injury to kidneys caused by exposure to paraquat ochratoxin A. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Perchloroethylene: Damage or injury to kidneys caused by exposure to a hydrocarbon called Perchloroethylene. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Pesticide solvents: Damage or injury to kidneys caused by exposure to pesticide solvents. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Pesticides: Damage or injury to kidneys caused by exposure to pesticides. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Platinum: Damage or injury to kidneys caused by exposure to platinum. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Polymyxin: Damage or injury to kidneys caused by a type of antibiotic called polymyxin. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Prostaglandin synthetase inhibitors: Damage or injury to kidneys caused by a type of analgesic called prostaglandin synthetase inhibitors. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Rifampin: Damage or injury to kidneys caused by a type of antibiotic called rifampin. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Silica: Damage or injury to kidneys caused by exposure to silica. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Silicon compounds: Damage or injury to kidneys caused by exposure to silicon compounds. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Silver: Damage or injury to kidneys caused by exposure to silver. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Solvents: Damage or injury to kidneys caused by exposure to solvents. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Styrene: Damage or injury to kidneys caused by exposure to a hydrocarbon called styrene. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Sulphonamides: Damage or injury to kidneys caused by sulphonamide antibiotics. The kidney damage usually occurs as a result of an allergic reaction to the antibiotic. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Thallium: Damage or injury to kidneys caused by exposure to thallium. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Toluene: Damage or injury to kidneys caused by exposure to a hydrocarbon called toluene. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Trichloroethane: Damage or injury to kidneys caused by exposure to a hydrocarbon called Trichloroethane. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Trichloroethylene: Damage or injury to kidneys caused by exposure to a hydrocarbon called trichloroethylene. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Trimethropin: Damage or injury to kidneys caused by a type of antibiotic called trimethropin. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - Uranium: Damage or injury to kidneys caused by exposure to Uranium. Often other organs and tissues are also affected but only the liver toxicity symptoms are listed below. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - analgesics: Damage or injury to kidneys caused by analgesics such as acetaminophen and nonsteroidal anti-inflammatory drugs. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage - antibiotics: Damage or injury to kidneys caused by antibiotics. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the toxicity. Kidney problems usually only occur with chronic use of the drug. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms.
• Kidney damage due to chemicals: Damage or injury to kidneys caused by substances such as chemicals and medicines. Often other organs and tissues are also affected but only the kidney toxicity symptoms are listed below. Symptoms vary depending on the degree of exposure and hence extent of the kidney damage or injury. Mild kidney damage may cause few if any symptoms whereas severe damage can ultimately result in kidney failure. Symptoms may be acute, subacute or chronic depending on the severity of the exposure. Factors such as age, dehydration and underlying kidney problems may also influence a person's risk of developing kidney problems and the severity of the symptoms. Occupational kidney damage is considered relatively uncommon due to current safe industrial practices.
• Kidney disease-Induced Hypertension: Kidney disease-Induced Hypertension is high blood pressure resulting from kidney diseases. The blood vessels to the kidney become narrowed or damaged which affects the ability of the blood to flow through them which in turn increases the blood pressure.
• Kidney symptoms: Symptoms affecting one or both kidneys.
• Kleeblattschaedel syndrome: A very rare syndrome characterized mainly by a head the is somewhat cloverleaf shaped.
• Klerat rodenticide poisoning: Klerat is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Kohl-induced lead poisoning: Kohl is a folk remedy used mainly by various ethnic groups (e.g. Africans, Asians, Indians and Pakistanis) to treat skin infections and to manage the umbilical stump. It is also used as a cosmetic in Arab communities. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Kosztolanyi syndrome: A very rare syndrome characterized mainly by severely retarded development, long thin fingers, mental retardation and skull and facial abnormalities.
• Koussef nichols syndrome: A very rare syndrome characterized mainly by muscle problems, a high body temperature and various other physical abnormalities.
• Kousseff-Nichols syndrome: A very rare syndrome characterized mainly by muscle problems, a high body temperature and various other physical abnormalities.
• Krabbe disease, atypical, due to saposin A deficiency: An inherited biochemical disorder which results in neurological regression within a few months of birth. Death usually occurs during the first few years of life. The disorder is similar to Krabbe disease but is differentiated by the genetic origin of the biochemical defect. Krabbe disease involves a defect in the galactocerebrosidase gene whereas atypical Krabbe disease involves a defect in the prosaposin gene which causes a deficiency of saposin A.
• Krabbe leukodystrophy: A rare inherited biochemical disorder involving the deficiency of an enzyme called galactocerebrosidase. It is a leukodystrophy which refers to a group of genetic disorders that affect the growth of the protective coating around the brain nerves.
• Krukenberg carcinoma: A form of ovarian cancer.
• Kugel-Stoloff syndrome: A rare form of heart disease that occurs in children and involves fibrosis and thickening of the heart muscle which affects it's ability to function. The cause is unknown.
• Kushta-induced lead poisoning: Kushta is a folk remedy used mainly by Indian and Pakistani people as an aphrodisiac and to treat diseases involving organs such as the liver, brain, heart and stomach. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Kyasanur-Forrest disease: A viral hemorrhagic fever that is transmitted to humans through tick bites. It is most prevalent in South Asia.
• L-3-alpha-hydroxyacyl-CoA dehydrogenase, short chain, deficiency: A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activity prevents some fats being converted into energy. Symptoms tend to be exacerbated during fasting as during fasting, the body tries to rely more heavily on fats for energy. Fatty acids that are not completely metabolized due to the enzyme deficiency may build up in various organs and cause serious complications.
• LADHSC deficiency: A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activity prevents some fats being converted into energy. Symptoms tend to be exacerbated during fasting as during fasting, the body tries to rely more heavily on fats for energy. Fatty acids that are not completely metabolized due to the enzyme deficiency may build up in various organs and cause serious complications.
• Labor, Premature: Labor that occurs before the pregnancy has reached full term i.e. before the 37th week of pregnancy. The degree of prematurity will determine the outcome of the infant.
• Lactic acidosis congenital infantile: A rare congenital condition where an infant has high levels of lactic acid in the blood causing metabolic acidosis.
• Langerhans cell sarcoma: A rare cancerous growth of Langerhans cells that can develop in the lymph nodes, skin, liver, spleen and bones.
• Lantana poisoning: Lantana is a small flowering shrub with spiny stems. It bears small clusters of colorful flowers on a stalk and small green fruit which become dark when ripe. The plant contains a chemical called triterpene which can cause poisoning symptoms if eaten. Death can occur if sufficient quantities are eaten as the chemical is quite toxic. The green berries are considered the most toxic part of the plant but the leaves are also poisonous but less likely to be eaten. Skin irritation can also result from skin contact with the plant.
• Larsen-like syndrome, lethal form: A very rare lethal syndrome characterized mainly by joint dislocations and breathing problems due to respiratory system abnormalities. The condition is a manifestation of abnormal collagen formation.
• Larsen-like syndrome, lethal type: A very rare lethal syndrome characterized mainly by joint dislocations and breathing problems due to respiratory system abnormalities.
• Laryngeal web congenital heart disease short stature: A very rare syndrome characterized mainly by short stature, congenital heart disease and an abnormal membrane of tissue across the larynx.
• Larynx symptoms: Symptoms affecting the larynx (voice box) in the neck
• Larynx, congenital partial atresia of: A birth defect where the larynx is obstructed. Usually a tracheostomy is required to permit normal breathing and prevent death.
• Lassa fever: Infectious rat-borne West African disease.
• Lateral body wall complex: A very rare syndrome characterized involving the absence of the whole or part of an arm or leg as well as a severe defect of the abdominal wall. Death often occurs at birth.
• Lead poisoning: A type of heavy metal poisoning caused by excessive exposure to lead.
• Lead poisoning - African Folk Remedies - Kohl: Kohl is a folk remedy used mainly by African people to treat skin infections and to manage the umbilical stump. It is also used as a cosmetic in Arab communities. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - African Folk Remedies - Surma: Surma is a black powder used as a cosmetic as well as a folk remedy by African people to treat teething. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Aisan Folk Remedies - Chuifong tokuwan: Chuifong tokuwan is a folk remedy used mainly by Asian people to arthritis and other pain. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Asian Folk Remedies - Bali goli: Bali goli (flat black bean) is a folk remedy used mainly by Asian people to treat intestinal problems. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Asian Folk Remedies - Deshi Dewa: Deshi Dewa is a folk remedy by Asian people as a fertility medicine. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Asian Folk Remedies - Ghasard: Ghasard is a lead-containing tetraoxide salt used mainly by Asian and Indian people as a tonic (usually for indigestion). This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Asian Folk Remedies - Kandu: Kandu (red powder) is a folk remedy used mainly by Asian people to treat intestinal problems. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Asian Folk Remedies - Kohl: Kohl is a folk remedy used mainly by Asian people to treat skin infections and to manage the umbilical stump. It is also used as a cosmetic in Arab communities. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Asian Folk Remedies - Pay-loo-ah: Pay-loo-ah is a folk remedy used mainly by Vietnamese people to treat fever and rash. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Asian Folk Remedies - Surma: Surma is a black powder used as a cosmetic as well as a folk remedy by Asian people to treat teething. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Chinese Folk Remedies - Ba Bow Sen: Ba Bow Sen is a folk remedy used mainly by Chinese people to treat childhood hyperactivity and to alleviate nightmares. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Chinese Folk Remedies - Cordyceps: Cordyceps is a folk remedy by Chinese people to treat high blood pressure, bleeding problems and diabetes. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Chinese Folk Remedies - Hai Ge Fen: Hai Ge Fen is clamshell powder used mainly by Chinese people to make traditional Chinese herbal medicines. This product has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Chinese Folk Remedies - Jin Bu Huan: Jin Bu Huan is a folk remedy used mainly by Chinese people to treat pain. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Chinese Folk Remedies - Po Ying Tan: Po Ying Tan is a folk remedy used mainly by Chinese people to treat minor childhood complaints. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Chinese Folk Remedies - Rueda: Rueda is a lead-containing folk remedy used mainly by Chinese people to treat infant colic or to calm young children. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Folk Remedies: A number of folk remedies have the potential to cause lead poisoning due to their relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. The high content of lead in some folk remedies can cause symptoms of lead poisoning which can result in serious illness and even death in severe cases.
• Lead poisoning - Hispanic Folk Remedies - Alarcon: Alarcon is a folk remedy used mainly by Hispanic people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Hispanic Folk Remedies - Azarcon: Azarcon is a lead-containing tetraoxide salt used mainly by Hispanic people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Hispanic Folk Remedies - Coral: Coral is a lead-containing tetraoxide salt used mainly by Hispanic people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Hispanic Folk Remedies - Greta: Greta is a lead-containing tetraoxide salt used mainly by Hispanic people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Hispanic Folk Remedies - Liga: Liga is a lead-containing tetraoxide salt used mainly by Hispanic people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Hispanic Folk Remedies - Luiga: Luiga is a folk remedy used mainly by Hispanic people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Hispanic Folk Remedies - Maria Luisa: Maria Luisa is a lead-containing tetraoxide salt used mainly by Hispanic people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Indian Folk Remedies - Deshi Dewa: Deshi Dewa is a folk remedy by Indian people as a fertility medicine. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Indian Folk Remedies - Kandu: Kandu (red powder) is a folk remedy used mainly by Indian people to treat intestinal problems. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Indian Folk Remedies - Kohl: Kohl is a folk remedy used mainly by Indian people to treat skin infections and to manage the umbilical stump. It is also used as a cosmetic in Arab communities. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Indian Folk Remedies - Kushta: Kushta is a folk remedy used mainly by the Indian people as an aphrodisiac and to treat diseases involving organs such as the liver, brain, heart and stomach. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Indian Folk Remedies - Surma: Surma is a black powder used as a cosmetic as well as a folk remedy by Indian people to treat teething. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Iranian Folk Remedies - Bint Al Zahab: Bint Al Zahab is a folk remedy used mainly by Iranian people to treat infant colic and to facilitate the passage of meconium in newborns. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Kuwait Folk Remedies - Bokhoor: Bokhoor is a traditional used mainly by Kuwait people to calm infants - it involves burning wood and lead sulphide and inhaling the fumes that are produced. This practice has the potential to cause lead poisoning due to the relatively high exposure to lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Loas Folk Remedies - Pay-loo-ah: Pay-loo-ah is a folk remedy used mainly by the Hmong people from Loas to treat fever and rash. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Mexican Folk Remedies - Alarcon: Alarcon is a folk remedy used mainly by Mexican people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Mexican Folk Remedies - Albayaidle: Albayaidle is a folk remedy used mainly by Mexican people to treat digestive or stomach problems such as vomiting and colic. It is also used to treat apathy and lethargy. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Mexican Folk Remedies - Albayalde: Albayalde is a folk remedy used mainly by Mexican people to treat digestive or stomach problems such as vomiting and colic. It is also used to treat apathy and lethargy. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Mexican Folk Remedies - Azarcon: Azarcon is a lead-containing tetraoxide salt used mainly by Mexican people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Mexican Folk Remedies - Coral: Coral is a folk remedy used mainly by Mexican people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Mexican Folk Remedies - Greta: Greta is a lead-containing tetraoxide salt used mainly by Mexican people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Mexican Folk Remedies - Liga: Liga is a lead-containing tetraoxide salt used mainly by Mexican people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Mexican Folk Remedies - Luiga: Luiga is a folk remedy used mainly by Mexican people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Mexican Folk Remedies - Maria Luisa: Maria Luisa is a lead-containing tetraoxide salt used mainly by Mexican people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Middle East Folk Remedies - Surma: Surma is a black powder used as a cosmetic as well as a folk remedy by Middle East people to treat teething. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Middle Eastern Folk Remedies - Alkohl: Alkohl is a folk remedy used mainly by Middle Eastern people to treat skin infections and to manage the umbilical stump. It is also used as a cosmetic in Arab communities. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Middle Eastern Folk Remedies - Anzroot: Anzroot is a folk remedy used mainly by Middle Eastern people to treat gastroenteritis. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Middle Eastern Folk Remedies - Cebagin: Cebagin is a folk remedy used mainly by Middle Eastern people to treat teething. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Middle Eastern Folk Remedies - Henna: Henna is used mainly by Middle Eastern people as a hair and skin dye. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Middle Eastern Folk Remedies - Kohl: Kohl is a folk remedy used mainly by Middle Eastern people to treat skin infections and to manage the umbilical stump. It is also used as a cosmetic in Arab communities. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Middle Eastern Folk Remedies - Saoot: Saoot is a folk remedy used mainly by Middle Eastern people to treat digestive eye injuries, teething and to manage the umbilical stump in newborns. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Pakistan Folk Remedies - Kohl: Kohl is a folk remedy used mainly by Pakistani people to treat skin infections and to manage the umbilical stump. It is also used as a cosmetic in Arab communities. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Pakistan Folk Remedies - Kushta: Kushta is a folk remedy used mainly by the Pakistani people as an aphrodisiac and to treat diseases involving organs such as the liver, brain, heart and stomach. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Pakistan Folk Remedies - Surma: Surma is a black powder used as a cosmetic as well as a folk remedy by Pakistani people to treat teething. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Pakistani eye cosmetics: Exposure to lead can result from the use of Pakistani eye cosmetics contaminated with lead. The most frequent cases have been noted in children as they are more sensitive to the effects of lead. Lead exposure can cause elevated levels of lead in the blood which in turn can cause various symptoms depending on the severity and duration of the exposure.
• Lead poisoning - Saudi Arabian Folk Remedies - Al Murrah: Al Murrah is a folk remedy used mainly by Saudi Arabian people to treat problems such as stomach pain, diarrhea and colic. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Saudi Arabian Folk Remedies - Bint Dahab: Bint Dahab is a folk remedy used mainly by Saudi Arabian people to treat such things as constipation, diarrhea, colic and various other infant conditions. It is also used by Saudi Arabian jewelers. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Saudi Arabian Folk Remedies - Bokhoor: Bokhoor is a traditional used mainly by Saudi Arabian people to calm infants - it involves burning wood and lead sulphide and inhaling the fumes that are produced. This practice has the potential to cause lead poisoning due to the relatively high exposure to lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Saudi Arabian Folk Remedies - Farouk: Farouk is a folk remedy by Saudi Arabian people to treat teething. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Saudi Arabian Folk Remedies - Santrinj: Santrinj is a paint primer but is also used as a folk remedy mainly by Saudi Arabian people to treat teething and gum boils. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Saudi Folk Remedies - Traditional Saudi medicine: Traditional Saudi medicine is a folk remedy used mainly by Saudi people to treat teething and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lead poisoning - Tamarind candy: Eating tamarind candy jam products made in Mexico can lead to exposure to lead as the product is often packaged in lead-containing containers which can leach lead. The most frequent cases have been noted in children as they are more sensitive to the effects of lead. Elevated levels of lead in the blood can cause various symptoms depending on the severity and duration of the exposure.
• Lead poisoning - Tibetan Folk Remedies - Tibetan herbal vitamin: Tibetan herbal vitamin is a folk remedy used mainly by Tibetan people to improve brain functioning. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Legionella adelaidensis infection: Legionella adelaidensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella anisa infection: Legionella anisa is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella beliardensis infection: Legionella beliardensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella birminghamensis infection: Legionella birminghamensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella bozemanii infection: Legionella bozemanii is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella bruneiensis infection: Legionella bruneiensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella brunensis infection: Legionella brunensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella busanensis infection: Legionella busanensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella cherrii infection: Legionella cherrii is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella cincinnatiensis infection: Legionella cincinnatiensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella donaldsonii infection: Legionella donaldsonii is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella donaldsonil infection: Legionella donaldsonil is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella drancourtii infection: Legionella drancourtii is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella drozanskii infection: Legionella drozanskii is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella dumofii infection: Legionella dumofii is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella erythra infection: Legionella erythra is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella fairfieldensis infection: Legionella fairfieldensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella fallonii infection: Legionella falloni is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella feelei infection: Legionella feelei is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella feeleii infection: Legionella feeleii is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella gesstiana infection: Legionella gesstiana is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella gormanii infection: Legionella micdadei is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella gratiana infection: Legionella gratiana is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella gresilensis infection: Legionella gresilensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella hackeliae infection: Legionella hackeliae is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella impletisoli infection: Legionella impletisoli is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella isrealensis infection: Legionella isrealensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella jamestowniensis infection: Legionella jamestowniensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella jordanis infection: Legionella jordanis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella lansingensis infection: Legionella lansingensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella londinensis infection: Legionella londinensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella longbeachae infection: Legionella longbeachae is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment, especially potting mixes and compost. Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella lytica infection: Legionella lytica is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella maceachemii infection: Legionella maceachemii is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella maceachernii infection: Legionella maceachernii is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella micdadei infection: Legionella micdadei is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella monrovica infection: Legionella monrovica is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella moravica infection: Legionella moravica is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella nautarum infection: Legionella nautarum is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella oakridgensis infection: Legionella oakridgensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella parisiensis infection: Legionella parisiensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella quateirensis infection: Legionella quateirensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella quinlivanii infection: Legionella quinlivanii is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella rowbothamii infection: Legionella rowbothamii is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella rubrilucens infection: Legionella rubrilucens is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella sainthelensi infection: Legionella sainthelensi is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella santicrucis infection: Legionella santicrucis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella shakespearei infection: Legionella shakespearei is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella spiritensis infection: Legionella spiritensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella steigerwaltii infection: Legionella steigerwaltii is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella tauriensis infection: Legionella tauriensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella tusconensis infection: Legionella tucsonensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella wadsorthii infection: Legionella wadsorthii is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella wadsworthii infection: Legionella wadsworthii is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella waltersii infection: Legionella moravica is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella worsliensis infection: Legionella worsliensis is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionella yabuuchiae infection: Legionella yabuuchiae is a type of bacteria which can cause infection in susceptible humans. Risk factors include diabetes, certain cancers, old age, immunosuppression, emphysema and smoking. Infection is rare and can occur at any age but the elderly or those with a weak immune system are more susceptible. These particular bacteria are commonly found in the environment (e.g. water and soil). Infection usually occurs through inhalation of the bacteria which results in a lung infection called pneumonia or may result in a flu-like illness. The bacteria may also cause respiratory system irritation, inflammation or sensitization. The nature and severity of symptoms may vary amongst patients. Some people may have the bacteria in their body but may have no symptoms. The incubation period lasts from 2 to 10 days but is usually 5 to 6 days. The infection cannot be transmitted from person to person.
• Legionnaires' disease: A severe respiratory disease which is caused by the Legionella pneumophila bacteria. The condition can result in pneumonia and can be life-threatening.
• Leishmaniasis: A rare infectious disease caused by any of a number of parasitic Leishmania species. Infection can cause any of three different manifestations: cutaneous leishmaniasis, mucosal leishmaniasis and visceral leishmaniasis.
• Lemierre's syndrome: A very rare condition where a throat infection leads to secondary infection and blood clot formation in the internal jugular vein. The infected blood clot can then travel to other parts of the body and cause problems. The usual bacterial culprit is Fusobacterium necrophorum.
• Lenz Majewski hyperostotic dwarfism: A rare genetic disorder characterized by dense, thick bones and symphalangism.
• Leptospirosis: Bacterial infection usually caught from animal urine.
• Lethal arthrogryposis with anterior horn cell disease: A lethal genetic disorder involving multiple contractures and facial abnormalities.
• Lethal arthrogryposis with anterior horn cell disease (LAAHD): A lethal disorder characterized by arthrogryposis and loss of anterior horn motor neurons which results in a lack of fetal movement.
• Lethal chondrodysplasia, Moerman type: A very rare lethal syndrome characterized mainly by abnormal bone development.
• Lethal chondrodysplasia, Seller type: A very rare lethal syndrome characterized mainly by angulated long bones and variation in bone density throughout the body.
• Lethal congenital contracture syndrome (LCCS): A rare inherited lethal disorder characterized by multiple congenital contractures. There are two main types caused by different genetic defects. Type 2 differs from type 1 in that it includes additional head, face and eye symptoms and hydrops, joint webbing and fractures were usually absent.
• Lethal congenital contracture syndrome 1: A rare inherited lethal disorder characterized by multiple congenital contractures. Type 1 occurs as a result of a genetic defect on chromosome 9q34.
• Leukemia, Lymphocytic, Acute, L1: Acute lymphocytic leukemia is a cancer of the white blood cells. Precursors to white blood cells are called blasts and are made by the bone marrow but in ALL the blasts are abnormal and do not develop into lymphocytes. Instead, the abnormal blasts or leukemic cells multiply rapidly and reduce the level of other types of blood cells such as red blood cells and platelets. There are three main subtypes (L1, L2 and L3) which are differentiated by the appearance of the cancerous cells: L1 is characterized by small, uniform cancer cells with a round nucleus and very little cytoplasm. L1 has a better prognosis than L2. L1 is the main form in children (about 85%) but is less common in adults (about 30%).
• Leukemia, Lymphocytic, Acute, L2: Acute lymphocytic leukemia is a cancer of the white blood cells. Precursors to white blood cells are called blasts and are made by the bone marrow but in ALL the blasts are abnormal and do not develop into lymphocytes. Instead, the abnormal blasts or leukemic cells multiply rapidly and reduce the level of other types of blood cells such as red blood cells and platelets. There are three main subtypes (L1, L2 and L3) which are differentiated by the appearance of the cancerous cells: L2 is characterized by larger cells, an irregular-shaped nucleus, more cytoplasm and significant variation between cells. L2 has a poorer prognosis than L1. L2 is the main form in adults (about 65%) but is less common in children (about 15%).
• Leukemia, Lymphocytic, Acute, L3: Acute lymphocytic leukemia is a relatively aggressive cancer of the white blood cells. Precursors to white blood cells are called blasts and are made by the bone marrow but in ALL the blasts are abnormal and do not develop into lymphocytes. Instead, the abnormal blasts or leukemic cells multiply rapidly and reduce the level of other types of blood cells such as red blood cells and platelets. There are three main subtypes (L1, L2 and L3) which are differentiated by the appearance of the cancerous cells. L3 is quite uncommon but is very similar to Burkitt's lymphoma - in fact, they may be considered the same disease with different manifestations.
• Leukemia, Myeloid, Philadelphia-Negative: Acute lymphocytic leukemia is a relatively aggressive cancer of the white blood cells. Precursors to white blood cells are called blasts and are made by the bone marrow but in ALL the blasts are abnormal and do not develop into lymphocytes. Instead, the abnormal blasts or leukemic cells multiply rapidly and reduce the level of other types of blood cells such as red blood cells and platelets. The Philadelphia negative form of the condition is not associated with a genetic mutation. It is distinguished from the positive form by the clinical course which is initially the same but progresses to eventual bone marrow failure without a distinct increase in blast cells. Other differences include poor response to chemotherapy, lower white blood cell counts, greater monocytosis, less basophilia, lower bone marrow myeloid to erythroid ratio and increased likelihood of developing thrombocytopenia. Philadelphia negative patients also tend to be older and median survival rates tend to be poorer.
• Leukemia, Myeloid, Philadelphia-Positive: Acute lymphocytic leukemia is a relatively aggressive cancer of the white blood cells. Precursors to white blood cells are called blasts and are made by the bone marrow but in ALL the blasts are abnormal and do not develop into lymphocytes. Instead, the abnormal blasts or leukemic cells multiply rapidly and reduce the level of other types of blood cells such as red blood cells and platelets. The Philadelphia form of myeloid leukemia carries the poorest prognosis of all the different types. It involves an acquired genetic mutation which results in the production tyrosine kinase which causes too many white blood cells to be produced which results in a shortage of other blood cell types. Treatment is aimed at inhibiting the production of tyrosine kinase.
• Leukemia, mast-cell: A very aggressive form of leukemia - a subtype of acute myeloid leukemia. The cancer can in rare cases develop from chronic myeloid leukemia or systemic mastocytosis but generally develops on its own.
• Leukocytoclastic angiitis - systemic: Inflammation of small blood vessels. Usually the small blood vessels in the ski are involved but sometimes small blood vessels in other organs such as joints, kidneys, and gastrointestinal tract may be involved. Symptoms become more serious once there is systemic (organ) involvement and death may result in some severe cases.
• Lhermitte-McAlpine syndrome: A type of neurodegenerative disorder that involves pyramidal and extrapyramidal symptoms. It can occur in middle-aged or old people and usually results in death within a year of onset.
• Liga-induced lead poisoning: Liga is a lead-containing tetraoxide salt used mainly by Mexican people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Limb transversal defect - cardiac anomaly: A very rare syndrome characterized mainly by heart anomaly and leg and hand malformations involving missing bones.
• Limbic encephalitis - neuromyotonia - hyperhidrosis - polyneuropathy: A rare autoimmune disorder involving excessive sweating, dysfunction central nervous system and neuromyotonia. The condition occurs when the body develops antibodies to voltage-gated potassium channels.
• Lion's mane jellyfish poisoning: The Lion's mane jellyfish is a large stinging jellyfish found in the colder waters of the Atlantic, Arctic and Pacific Oceans. The jellyfish can deliver a painful sting with skin burning and blistering. Prolonged skin exposure can result in breathing problems, muscle cramps and even death.
• Liposarcoma: A rare malignant tumor of fat cells. Usually affects thighs in women over 30 years of age.
• Lissencephaly, X-linked 2: A rare brain malformation where the surface of the brain is smoother than normal. Genital anomalies are also associated. The severity of the disorder is variable.
• Lissencephaly, X-linked, 1: Abnormal brain development resulting in an abnormally smooth brain surface which results in neurological symptoms such as mental retardation. This particular type is inherited in a X-linked manner is caused by a defect in the doublecortin gene on chromosome Xq22.3-q23.
• Lissencephaly, type 1, X-linked: Abnormal brain development characterized by an abnormally smooth brain. This form of the disorder is inherited in a X-linked manner (defect on the DCX gene) and the corpus callosum fails to develop. Males tend to be affected more severely than females.
• Listeriosis: Bacterial food poisoning
• Liver cancer: The occurrence of malignancy that occurs in the liver
• Liver failure: When the liver fails to function
• Lizard poisoning: A few lizard species are venomous e.g. Gila monster and Mexican beaded lizard. Envenomation by lizards is very uncommon but these venomous lizards can cause life-threatening symptoms. Gila lizards tend to hold on with their jaws while biting and the longer the jaws remain attached to the skin, the more severe the poisoning may be.
• Lobstein disease: A group of rare inherited diseases that involves fragile bones. There are many different types based on the severity and extent of symptoms. Some types are severe enough to cause stillbirth or infant death whereas other types may cause few if any problematic symptoms.
• Local anaesthetic allergy: Using Local anaesthetic can cause an allergic response in some people however this is considered rare. It involves the body's immune system overreacting to the drug. The type and severity of symptoms can vary considerable though skin symptoms are the most common allergic response to drugs.
• Long QT syndrome type 10: A genetic heart disorder characterized by an abnormal heart rhythm (long Q-T interval) where the heart takes longer than normal to recharge between beats. The severity of the condition can vary. Type 10 is distinguished from other types by the origin of the genetic defect (SCN4B gene on chromosome 11q23).
• Long QT syndrome type 11: A genetic heart disorder characterized by an abnormal heart rhythm (long Q-T interval) where the heart takes longer than normal to recharge between beats. The severity of the condition can vary. Type 11 is distinguished from other types by the origin of the genetic defect (chromosome 7q21-q22).
• Long QT syndrome type 2: A genetic heart disorder characterized by an abnormal heart rhythm (long Q-T interval) where the heart takes longer than normal to recharge between beats. The severity of the condition can vary. Type 3 is distinguished from other types by the origin of the genetic defect (chromosome 7).
• Long QT syndrome type 3: A genetic heart disorder characterized by an abnormal heart rhythm (long Q-T interval) where the heart takes longer than normal to recharge between beats. The severity of the condition can vary. Type 3 is distinguished from other types by the origin of the genetic defect (chromosome 3p21).
• Long QT syndrome type 4: A very rare genetic heart disorder characterized by an abnormal heart rhythm (long Q-T interval) where the heart takes longer than normal to recharge between beats. The severity of the condition can vary. Type 4 is distinguished from other types by the origin of the genetic defect (gene for Ankyrin B on chromosome 4q25-q27).
• Long QT syndrome type 5: A genetic heart disorder characterized by an abnormal heart rhythm (long Q-T interval) where the heart takes longer than normal to recharge between beats. The severity of the condition can vary. Type 5 is distinguished from other types by the origin of the genetic defect (KCNE1 gene on chromosome 21q22.1-q22.2).
• Long QT syndrome type 6: A genetic heart disorder characterized by an abnormal heart rhythm (long Q-T interval) where the heart takes longer than normal to recharge between beats. The severity of the condition can vary. Type 6 is distinguished from other types by the origin of the genetic defect (KCNE2 gene on chromosome 21q22.1).
• Long QT syndrome type 9: A genetic heart disorder characterized by an abnormal heart rhythm (long Q-T interval) where the heart takes longer than normal to recharge between beats. The severity of the condition can vary. Type 9 is distinguished from other types by the origin of the genetic defect (caveolin 3 gene on chromosome 3p25).
• Long QT syndrome, familial: A familial heart condition which is characterized by prolongation of the QT interval of the heart rhythm. Exercise or excitement can exacerbate symptoms.
• Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency: A rare inherited genetic condition where the body is unable to convert certain fats to energy i.e. there is not enough of a certain enzyme (3-hydroxyacyl-coenzyme A dehydrogenase) which is needed to metabolize a type of fat called long-chain fatty acids. The build-up of these fatty acids in the body causes damage.
• Loquat poisoning: Loquat is a shrubby plant which bears clusters of small white flowers and largish yellow fleshy fruit. The plant is often used in gardens as an ornamental plant. The kernel from inside the seeds contains a chemical called cyanogenic glycoside which can be poisonous if eaten in large quantities. The fruit from the plant is actually safe to eat but the seeds should be avoided.
• Lortab overdose: Lortab is a prescription drug used to treat. Excessive doses of the drug can result in various symptoms and even death in severe cases.
• Lovastatin - Teratogenic Agent: There is evidence to indicate that exposure to Lovastatin during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
• Lower limb anomaly - ureteral obstruction: A very rare syndrome characterized mainly by an obstructed ureter and a leg anomaly.
• Luiga-induced lead poisoning: Coral is a folk remedy used mainly by Mexican people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Lurie-Kletsky syndrome: A very rare syndrome characterized mainly by a buildup of fluid inside the skull, abnormal brain development (corpus callosum) and a diaphragmatic hernia.
• Lymphangiectasies and lymphedema Hennekam type: A rare disorder characterized by buildup of lymphatic fluid in the limbs, face and genitals, seizures and mental and growth retardation.
• Lymphatic neoplasm: A tumor that develops in lymphatic tissue. The tumor may be cancerous or benign.
• Lymphoedema - lymphangiectasia - mental retardation: A rare disorder characterized by buildup of lymphatic fluid in the limbs, face and genitals, seizures and mental and growth retardation.
• Lymphoid interstitial pneumonia: A relatively rare form of lung disease characterized by the buildup of lymphocytes (a type of white blood cell) in the air spaces or alveoli of the lungs. The condition can affect children or adults and is frequently associated with conditions such as HIV and autoimmune conditions such as rheumatoid arthritis and Hashimoto's thyroiditis. Symptoms may develop gradually over a period of months or even years in some cases.
• Lymphoma, Large-Cell, Follicular: A cancer of cells in the immune system. The cancer is comprised of large cells and tends to be aggressive and metastasizes readily.
• Lymphoma, large-cell: A cancer of cells in the immune system. The cancer is comprised of large cells and tends to be aggressive and metastasizes readily.
• Lymphoma, large-cell, immunoblastic: A cancer of the immune system characterized by the presence of immunoblasts. Immunoblasts are T cells which have been transformed due to stimulation by an antigen.
• Lymphomatoid Granulomatosis: A rare, progressive blood vessel disease where nodular lesions destroy blood vessels - lungs, skin and nervous system are mainly involved.
• Lysosomal glycogen storage disease with normal acid maltase activity: A rare inherited disorder characterized by severe heart problems, varying degrees of muscle weakness and often mental retardation. Other symptoms such as mental retardation may also occur. The genetic anomaly manifests as a deficiency of a protein called LAMP-2 (Lysosomal-Associated Membrane Protein 2) which affects lysosomes.
• Lysteria monocytoigeneses meningitis: A very rare form of meningitis (bacterial infection of the brain membrane or meninges) caused by Listeria monocytogenes. The condition is more common in the elderly and those with poor immune system and death is common.
• M/SCHAD deficiency: A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activity prevents some fats being converted into energy. Symptoms tend to be exacerbated during fasting as during fasting, the body tries to rely more heavily on fats for energy. Fatty acids that are not completely metabolized due to the enzyme deficiency may build up in various organs and cause serious complications.
• MHC class 1 or class 2 deficiency: An inherited immunodeficiency disorder involving a deficiency of class I and II major histocompatibility complexes. Serious infections can result.
• MacDermot-Winter syndrome: A very rare syndrome characterized mainly by a small head, underdeveloped genitalia and a protrusion of the area between the eyes (glabella).
• Machado-Joseph Disease: Rare genetic muscle disease causing muscle weakness.
• Malaria: A parasitic disease transmitted through mosquito bites.
• Malformations in neuronal migration: A rare disorder where the brain fails to develop normally - usually the cerebral cortex is involved. Various parts of the brain can be affected to various degrees depending on what stage of development the defect occurs. Mental retardation is one of the most common symptoms associated with brain malformations.
• Malignant Teratocarcinosarcoma: A rare type of cancer that involves connective (bone, cartilage, fat) and epithelial (skin and lining of internal organs) tissue and tends to be of a large size. It often tends to occur in the nose, pharynx and sinus areas. Symptoms are determined by the size and location of the tumor.
• Malignant germ cell tumor: Malignant tumors that are made up of germ cells which are immature cells that eventually become reproductive system tissues in males and females. The symptoms depend on the location of the tumor which may occur in the ovaries, testes or anywhere along the body's midline such as the chest, head, abdomen, pelvis and lower back.
• Malignant hypertension: Malignant hypertension is a condition characterized by very high blood pressure and swelling of the optic nerve. This type of hypertension is more common in people with kidney problems such as narrowed kidney blood vessels. The condition is a medical emergency which can cause organ damage if not treated promptly.
• Malignant hyperthermia susceptibility type 1: A rare, potential lethal disorder that is triggered by general anesthetic or certain muscle relaxant drugs. On exposure to the drugs, muscle metabolism is severely disrupted and the body is unable to control its temperature which can lead to death without treatment. The chromosomal defect for type 1 is located at 19q13.1.
• Malignant hyperthermia susceptibility type 2: A rare, potential lethal disorder that is triggered by general anesthetic or certain muscle relaxant drugs. On exposure to the drugs, muscle metabolism is severely disrupted and the body is unable to control its temperature which can lead to death without treatment. The chromosomal defect for type 2 is located at 17q11.2-q24.
• Malignant hyperthermia susceptibility type 3: A rare, potential lethal disorder that is triggered by general anesthetic or certain muscle relaxant drugs. On exposure to the drugs, muscle metabolism is severely disrupted and the body is unable to control its temperature which can lead to death without treatment. The chromosomal defect for type 3 is located at 7q21-q22.
• Malignant hyperthermia susceptibility type 4: A rare, potential lethal disorder that is triggered by general anesthetic or certain muscle relaxant drugs. On exposure to the drugs, muscle metabolism is severely disrupted and the body is unable to control its temperature which can lead to death without treatment. The chromosomal defect for type 4 is located at 3q13.1.
• Malignant hyperthermia susceptibility type 5: A rare, potential lethal disorder that is triggered by general anesthetic or certain muscle relaxant drugs. On exposure to the drugs, muscle metabolism is severely disrupted and the body is unable to control its temperature which can lead to death without treatment. The chromosomal defect for type 5 is located at 1q32.
• Malignant hyperthermia susceptibility type 6: A rare, potential lethal disorder that is triggered by general anesthetic or certain muscle relaxant drugs. On exposure to the drugs, muscle metabolism is severely disrupted and the body is unable to control its temperature which can lead to death without treatment. The chromosomal defect for type 6 is located at 5p.
• Malignant mesenchymal tumor: A malignant tumor that arises from soft tissue. Symptoms are determined by the size and location of the tumor. It is a usually aggressive tumor that can occur muscle, fat, bone and blood vessels.
• Malignant mixed Mullerian tumor: A rare malignant cancer that develops in the uterus, ovary or fallopian tubes. The tumor contains epithelial and stromal cells. The cancer may be slow-growing or aggressive and may metastasize.
• Malignant rhabdoid tumors: An aggressive malignant tumor that occurs in children. Symptoms depend on the location of the tumor. The tumors often form in the kidneys and then tend to metastasize to the brain and sometimes the lungs. Symptoms will vary depending on the location of the tumor.
• Mandibuloacral dysplasia: A very rare syndrome characterized mainly by a prematurely aged appearance and bone abnormalities. There are two subtypes with type B involving loss of fat layers under the skin mainly in the extremities, face and trunk whereas type A involves mainly the extremities. The severity of the symptoms is variable.
• Mandibuloacral dysplasia with type A lipodystrophy: A very rare syndrome characterized mainly by a prematurely aged appearance and bone abnormalities. Loss of fat layers under the skin occurs mainly in the extremities in type B. The severity of the symptoms is variable.
• Mandibuloacral dysplasia with type B lipodystrophy: A very rare syndrome characterized mainly by a prematurely aged appearance and bone abnormalities. Loss of fat layers under the skin occurs mainly in the extremities, face and trunk in type B. The severity of the symptoms is variable.
• Marburg virus: Serious virus related to Ebola.
• Mareck's disease - nervous system: A viral disease that affects poultry - it is very contagious and is a herpes virus. The virus tends to affect the nerves and cause tumors in internal organs. Poultry may be unable to lay eggs or may even die. Young birds are more susceptible than older birds with death most common between the ages of 8 and 20 weeks. The virus may attack the nervous system and result in paralysis or it may attack the visceral system and cause tumors in the internal organs. Some birds may die without any obvious symptoms.
• Mareck's disease - visceral: A viral disease that affects poultry - it is very contagious and is a herpes virus. The virus tends to affect the nerves and cause tumors in internal organs. Poultry may be unable to lay eggs or may even die. Young birds are more susceptible than older birds with death most common between the ages of 8 and 20 weeks. The virus may attack the nervous system and result in paralysis or it may attack the visceral system and cause tumors in the internal organs. Some birds may die without any obvious symptoms.
• Marek disease: A viral disease that affects poultry - it is very contagious and is a herpes virus. The virus tends to affect the nerves and cause tumors in internal organs. Poultry may be unable to lay eggs or may even die. Young birds are more susceptible than older birds with death most common between the ages of 8 and 20 weeks. The virus may attack the nervous system and result in paralysis or it may attack the visceral system and cause tumors in the internal organs. Some birds may die without any obvious symptoms.
• Marek's disease: A viral disease that affects poultry - it is very contagious and is a herpes virus. The virus tends to affect the nerves and cause tumors in internal organs. Poultry may be unable to lay eggs or may even die. Young birds are more susceptible than older birds with death most common between the ages of 8 and 20 weeks. The virus may attack the nervous system and result in paralysis or it may attack the visceral system and cause tumors in the internal organs. Some birds may die without any obvious symptoms.
• Marfan Syndrome type 2: A very rare syndrome characterized by some of the skeletal and heart blood vessel abnormalities seen in Marfan syndrome but there are no eye abnormalities. The genetic cause of the two types is different.
• Marfan syndrome: A genetic connective tissue disorder involving a defect of chromosome 15q21.1 which affects the production of the fibrillin needed to make connective tissue.
• Marfan-like syndrome, Boileau type: A rare disorder that is similar to Marfan syndrome but tends to only involve skeletal and cardiovascular symptoms and signs.
• Maria Luisa-induced lead poisoning: Maria Luisa is a lead-containing tetraoxide salt used mainly by Mexican people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Marine turtle poisoning: Marine turtles are found and eaten in the rivers and coastal waters of Southeast Asia. It is believed that sometimes these turtles become poisonous when the eat toxic algae which occur at certain times of the year. Symptoms vary in nature and severity amongst patients - obviously the more that is eaten, the more severe the symptoms are.
• Marine turtle poisoning - Green Sea Turtle: Green Sea turtles are found and eaten in the rivers and coastal waters of Southeast Asia. It is believed that sometimes these turtles become poisonous when the eat toxic algae which occur at certain times of the year. Symptoms vary in nature and severity amongst patients - obviously the more that is eaten, the more severe the symptoms are.
• Marine turtle poisoning - Hawksbill Turtle: Hawksbill turtles are found and eaten in the rivers and coastal waters of Southeast Asia. It is believed that sometimes these turtles become poisonous when the eat toxic algae which occur at certain times of the year. Symptoms vary in nature and severity amongst patients - obviously the more that is eaten, the more severe the symptoms are.
• Marine turtle poisoning - Leatherback Turtle: Leatherback turtles are found and eaten in the rivers and coastal waters of Southeast Asia. It is believed that sometimes these turtles become poisonous when the eat toxic algae which occur at certain times of the year. Symptoms vary in nature and severity amongst patients - obviously the more that is eaten, the more severe the symptoms are.
• Marine turtle poisoning - Loggerhead Turtle: Loggerhead turtles are found and eaten in the rivers and coastal waters of Southeast Asia. It is believed that sometimes these turtles become poisonous when the eat toxic algae which occur at certain times of the year. Symptoms vary in nature and severity amongst patients - obviously the more that is eaten, the more severe the symptoms are.
• Marine turtle poisoning - Soft-shelled Turtle: Soft-shelled turtles are found and eaten in the rivers and coastal waters of Southeast Asia. It is believed that sometimes these turtles become poisonous when the eat toxic algae which occur at certain times of the year. Symptoms vary in nature and severity amongst patients - obviously the more that is eaten, the more severe the symptoms are.
• Maroteaux-Stanescu-Cousin syndrome: A very rare lethal syndrome characterized mainly by abnormal bone development.
• Marseilles fever: An infectious disease that is caused by Rickettsia conorii which is transmitted by the brown dog tick (Rhipicephalus sanguineus). The disease occurs predominantly in Mediterranean areas such as India and Africa. The onset of symptoms is usually sudden and the incubation period is usually between 6 and 10 days.
• Matikus rodenticide poisoning: Matikus is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Mayapple poisoning: The Mayapple is a small flowering plant which is often found growing naturally. It bears small single flowers and apple-like fruit which turns yellow when ripe. The unripe fruit and leaves contain a chemical called podophyllin which can cause poisoning if eaten. The plant is considered highly toxic and death can occur if sufficient quantities are eaten. The leaves, roots and unripe fruit are toxic but the ripe fruit is edible. The plant has been used to treat venereal warts.
• Measles: Once common viral infection now rare due to vaccination.
• Measles Encephalitis in Children with Immunosuppression: A rare complication of the measles virus. Some patients with a history of measles before the age of two develop progressive brain inflammation. The condition is rare and tends to only occur only in immunosuppressed children e.g. those who have acute lymphocytic leukemia. Symptoms may develop suddenly and tends to occur from weeks to months after the measles has resolved.
• Meckel syndrome type 2: A very rare lethal syndrome characterized mainly by kidney and liver abnormalities, extra fingers and a gap in the back of the skull through which some brain matter protrudes.
• Meckel syndrome type 3: A very rare lethal syndrome characterized mainly by kidney and liver abnormalities, extra fingers and a gap in the back of the skull through which some brain matter protrudes. Type 3 differs from the other types in the location of the genetic defect and by the fact that meningoencephaloceles and extra fingers tend to occur less frequently.
• Meconium aspiration syndrome: A condition that occurs when an infant suffers respiratory distress following birth due to the presence of meconium in the amniotic fluid.
• Mediastinal endodermal sinus tumors: A rare yolk sac tumor that occurs in the mediastinal area (the area that separates the lungs). It is a type of cancer that originates from immature cells (germ cells) that evolve into gonadal tissue but can also be found in other parts of the body such as the chest. The tumors tend to be quite aggressive and often metastasize.
• Mediastinitis: inflammation of the tissues in the mid-chest, or mediastinum
• Mediterranean myoclonic epilepsy: A rare inherited type of progressive myoclonus epilepsy which tends to cause symptoms during childhood. The involuntary muscle movements tend to occur more frequently and become more severe with increasing age. Symptoms may occur following various stimuli such as light, stress or exercise.
• Medium and long chan 3-hydroxyacyl-coenzyme A dehydrogenase deficiency: A metabolic disorder characterized by the deficiency of an enzyme (3-hydroxyacyl-coenzyme A dehydrogenase) which is needed to metabolise long and medum-chain fatty acids. The severity of symptoms may vary depending on the degree of the deficiency.
• Medium and short chain 3-hydroxyacyl-CoA dehydrogenase deficiency: A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activity prevents some fats being converted into energy. Symptoms tend to be exacerbated during fasting as during fasting, the body tries to rely more heavily on fats for energy. Fatty acids that are not completely metabolized due to the enzyme deficiency may build up in various organs and cause serious complications.
• Megacystis microcolon - intestinal hypoperistalsis - hydronephrosis: A rare and usually lethal gastrointestinal disorder involving dysfunction of the bowel and bladder due to abnormalities of the smooth muscle.
• Melanoma - astrocytoma syndrome: A rare syndrome characterized by the association of a melanoma with a type of brain tumor called an astrocytoma. The exact symptoms may vary depending on the exact location of the brain tumor.
• Melioidosis: Bacterial infection from soil or water.
• Mendelian susceptibility to atypical mycobacteria: A very rare group of disorders where a person without an immune deficiency is susceptible to infection by weak mycobacterial organisms, nontuberculous and environmental mycobacteria e.g. Calmette-Guerin Bacillus (BCG). The severity of the disorder is greatly variable and ranges from a localized recurring non-tuberculous mycobacterial infection to a potentially fatal BCG infection. Most people who are infected with these organisms have no symptoms but a genetic mutation in some people makes them more susceptible.
• Mendelson syndrome: Symptoms caused by breathing in gastric juices stomach contents during general anesthesia. Severe cases can lead to shock and death but this is rare. The condition is believed to be caused by the absence of laryngeal reflexes. It is most often seen in pregnant women.
• Meningitis: Infection of the membrane around the brain (as a symptom)
• Meningococcal disease: Dangerous bacterial infection causing meningitis or bacteremia.
• Meningococcal infection: A rare infectious disease caused by a bacterium called Neisseria meningitides.
• Meningococcemia: A rare infectious disease whose main symptoms are upper respiratory tract infection, fever, rash and eye and ear problems.
• Mental retardation - myopathy - short stature - endocrine defect: A very rare syndrome characterized mainly by mental retardation, muscle disease, short stature and endocrine defects.
• Mental retardation, X-linked, Pai type: A rare X-linked disorder characterized by mental retardation and a slightly unusual facial appearance. The disorder is inherited in a X-linked manner which means that only males display the full range of symptoms whereas female carriers may have mild or no symptoms.
• Mercury poisoning: A type of heavy metal poisoning caused by excessive exposure to mercury.
• Mercury poisoning - Folk Remedies: Various folk remedies and medicines contain inorganic mercury and mercury salts. They can lead to mercury poisoning and severe cases can result in death. Children tend to be more sensitive to the effects of mercury poisoning than adults. Even low levels of exposure can cause neurological symptoms in infants and young children. Fetal exposure to mercury can also result in symptoms.
• Mercury poisoning - consumption of contaminated fish: Eating fish contaminated with mercury can lead to mercury poisoning in humans. The severity and range of symptoms experienced can vary greatly depending on the level and duration of exposure. Severe poisoning can lead to death. Pregnant women who eat mercury contaminated fish may give birth to infants who suffer symptoms such as ataxia, tremors, seizures, mental retardation and cerebral palsy. An epidemic was reported where hundreds of Japanese villagers suffered mercury poisoning after eating fish contaminated by a nearby factory. Nearly half of the victims eventually died and children born during that period suffered a variety of neurological problems.
• Mesangial sclerosis, diffuse: A rare inherited disorder involving a kidney disorder that starts early in life and rapidly progresses to kidney failure. Death often occurs within years of birth.
• Mesothelioma: Type of lung cancer associated with asbestos.
• Metachromatic Leukodystrophy: An inherited biochemical deficiency involving a deficiency of the enzyme called arylsulfatase A which leads to a harmful buildup of fatty material in the body.
• Metal Fume Fever - Aluminium: Metal fume fever is a flu-like illness which can result from inhalation of aluminium oxide fumes. The condition is most likely to occur in poorly ventilated areas in the metal-working industry.
• Metal Fume Fever - Antimony: Metal fume fever is a flu-like illness which can result from inhalation of antimony fumes. The condition is most likely to occur in poorly ventilated areas in the metal-working industry.
• Metal Fume Fever - Cadmium: Metal fume fever is a flu-like illness which can result from inhalation of cadmium fumes. The condition is most likely to occur in poorly ventilated areas in the metal-working industry.
• Metal Fume Fever - Chromium: Metal fume fever is a flu-like illness which can result from inhalation of chromium fumes. The condition is most likely to occur in poorly ventilated areas in the metal-working industry.
• Metal Fume Fever - Copper: Metal fume fever is a flu-like illness which can result from inhalation of copper fumes. The condition is most likely to occur in poorly ventilated areas in the metal-working industry.
• Metal Fume Fever - Iron: Metal fume fever is a flu-like illness which can result from inhalation of iron fumes. The condition is most likely to occur in poorly ventilated areas in the metal-working industry.
• Metal Fume Fever - Magnesium: Metal fume fever is a flu-like illness which can result from inhalation of magnesium fumes. The condition is most likely to occur in poorly ventilated areas in the metal-working industry.
• Metal Fume Fever - Manganese: Metal fume fever is a flu-like illness which can result from inhalation of manganese fumes. The condition is most likely to occur in poorly ventilated areas in the metal-working industry.
• Metal Fume Fever - Nickel: Metal fume fever is a flu-like illness which can result from inhalation of nickel fumes. The condition is most likely to occur in poorly ventilated areas in the metal-working industry.
• Metal Fume Fever - Selenium: Metal fume fever is a flu-like illness which can result from inhalation of selenium fumes. The condition is most likely to occur in poorly ventilated areas in the metal-working industry.
• Metal Fume Fever - Silver: Metal fume fever is a flu-like illness which can result from inhalation of silver fumes. The condition is most likely to occur in poorly ventilated areas in the metal-working industry.
• Metal Fume Fever - Tin: Metal fume fever is a flu-like illness which can result from inhalation of tin fumes. The condition is most likely to occur in poorly ventilated areas in the metal-working industry.
• Metal Fume Fever - Zinc: Metal fume fever is a flu-like illness which can result from inhalation of zinc fumes. The condition is most likely to occur in poorly ventilated areas in the metal-working industry.
• Metal fume fever: Metal fume fever is a flu-like illness which can result from inhalation of iron oxide fumes. The condition is most likely to occur in poorly ventilated areas in the metal-working industry.
• Metastatic squamous neck cancer with occult primary: A type of cancer that occurs in the neck and has spread (metastasized) to the lymph nodes from a primary source that has not been able to be determined. Squamous cells are cells that line hollow organs as well as the skin and throat.
• Metatropic dwarfism: A rare genetic disorder characterized by extremely small stature, short limbs and skeletal abnormalities.
• Methadone - Teratogenic Agent: There is evidence to indicate that exposure to Methadone during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
• Methadone overdose: Methadone is a prescription drug mainly used as a painkiller and to treat heroin addiction. Excessive doses of the drug can result in various symptoms and even death in severe cases.
• Methamphetamine overdose: Methamphetamine is a prescription drug mainly used to treat ADHD . Excessive doses of the drug can result in various symptoms and even death in severe cases.
• Methotrexate toxicity: The toxic reaction of the body to the substance, possibly via allergic reaction or overdose.
• Methyldopa-induced Immune Hemolytic Anemia: Methyldopa-induced immune hemolytic anemia is a condition where use of a medication called Methyldopa triggers the body's immune system to destroy it's own red blood cells which results in anemia.
• Methylene tetrahydrofolate reductase deficiency: A inborn error of metabolism where an inherited deficiency of methylene tetrahydrofolate reductase causes symptoms of ranging severity - from asymptomatic to severe neurological degeneration and premature death.
• Methylmalonic acidemia - homocystinuria: A rare inborn error of metabolism which results in impaired vitamin B12 metabolism. There are a number of forms of this condition with variable severity.
• Methylmalonic acidemia, Cobalamin B deficiency: An inherited organic acid disorder where an enzyme deficiency (Cobalamin B deficiency) impairs the body's ability to break down certain proteins (methionine, threonine, isoleucine and valine) consumed in the diet. This results in a buildup of glycine and methylmalonic acid which results in harmful affects.
• Methylmalonic acidemia, Methylmalonyl CoA mutase deficiency: An inherited organic acid disorder where an enzyme (Methylmalonyl CoA mutase apoenzyme) deficiency impairs the body's ability to break down certain proteins (methionine, threonine, isoleucine and valine) consumed in the diet. This results in a buildup of glycine and methylmalonic acid which results in harmful affects.
• Methylmalonic acidemia, cobalamin A deficiency: An inherited organic acid disorder where an enzyme deficiency (Cobalamin A deficiency) impairs the body's ability to break down certain proteins (methionine, threonine, isoleucine and valine) consumed in the diet. This results in a buildup of glycine and methylmalonic acid which results in harmful affects.
• Methylmalonic acidemia, methylmalonyl CoA racemase deficiency: An inherited organic acid disorder where an enzyme (methylmalonyl CoA racemase) deficiency impairs the body's ability to break down certain proteins (methionine, threonine, isoleucine and valine) consumed in the diet. This results in a buildup of glycine and methylmalonic acid which results in harmful affects.
• Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl: An inherited organic acid disorder where an enzyme deficiency impairs the body's ability to break down certain proteins (methionine, threonine, isoleucine and valine) consumed in the diet. This results in a buildup of glycine and methylmalonic acid which results in harmful affects. The disorder results from a combined synthesis defect of AdoCbl and MeCbl.
• Methylmalonic aciduria - homocystinuria: A rare group of disorders characterized by methylmalonic aciduria and homocystinuria resulting from abnormal metabolism of vitamin B12 by the liver. There are various subtypes of the condition with varying ages of onset and severity of symptoms.
• Methylmalonicaciduria with homocystinuria, cobalamin F: An inherited organic acid disorder where an enzyme deficiency (cbl F) impairs the body's ability to break down certain proteins (methionine, threonine, isoleucine and valine) consumed in the diet. This results in a buildup of methylmalonic acid and homocystine which results in harmful affects.
• Methylmalonicaciduria, vitamin B12 unresponsive, mut 0: A metabolic disorder whose severity is somewhat variable - most patients die within months of birth with survivors having neurological problems. The condition involves abnormal metabolism of vitamin B12 which doesn't respond to treatment using vitamin B12 administration. This disorder is more severe than the mut (-) form
• Mexican Beaded Lizard poisoning: Gila lizards are one of the few venomous species of lizard. They are found in parts of America such as Arizona, California, Nevada and Mexico. Envenomation by lizards is very uncommon but these venomous lizards can cause life-threatening symptoms. Gila lizards tend to hold on with their jaws while biting and the longer the jaws remain attached to the skin, the more severe the poisoning may be.
• Mexican tea poisoning: Mexican tea is plant that bears elongated clusters of small green flowers and small greenish fruit which contain seeds which are green when fresh and black when dry. The plant has a strong odor. The oil in the seeds contain chemicals (including terpene peroxide ascaride) which are very poisonous and cause death if sufficient quantities are eaten. The oil from the seeds is often used to control worm infestations in livestock.
• Micrencephaly corpus callosum agenesis: A very rare disorder characterized by abnormal brain development which results in a very small brain. Patients may die during infancy and survivors suffer mental retardation and other physical abnormalities.
• Micrencephaly olivopontocerebellar hypoplasia: A rare fatal condition characterized by brain disease and a small underdeveloped brain.
• Microcephalic osteodysplastic primordial dwarfism types 1 and 3: Microcephalic osteodysplastic primordial dwarfism types 1 and 3 were originally regarded as separate conditions but it was recently concluded that they were different expressions of the same condition. The main differences between the two forms is a difference in the radiological bone anomalies. The condition is characterized mainly by bone abnormalities, short stature and a small head.
• Microcephaly - pontocerebellar hypoplasia - dyskinesia: A rare, recessively inherited disorder characterized by an abnormally small brain and brainstem which manifests as a small head and mental retardation. The brain progressively degenerates.
• Microcephaly brain defect spasticity hypernatremia: A rare syndrome characterized mainly by a small head, brain defect, spasticity and high sodium level.
• Microcephaly immunodeficiency lymphoreticuloma: A very rare syndrome characterized mainly by a small head, reduced immunity and increased risk of cancer. There are a wide range of other abnormalities and symptoms that can occur.
• Microcephaly, Amish type: A very rare lethal condition characterized by an abnormally small head and a metabolic abnormality.
• Microcephaly, primary autosomal recessive: A rare, recessively inherited condition characterized by a small head. The 6 forms of this condition differ with respect to the origin of the genetic defect involved. The size of the brain often reduces in size with age with many cases resulting in death before the age of 30 years.
• Microlissencephaly: An abnormally smooth brain as well as a very small head. The brain fails to develop normally leading to serious abnormalities.
• Microlissencephaly - micromelia: A rare syndrome characterized mainly by short arms, a brain defect called microlissencephaly, small head and early death.
• Micromelic bone dysplasia with cloverleaf skull: A rare disorder characterized by a cloverleaf skull deformity, small limbs and bone abnormalities of the chest and spine. The disorder is lethal.
• Microphthalmia syndromic, type 9: A rare inherited disorder characterized by small or absent eyes and lung, heart and diaphragmatic abnormalities. The disorder is caused by a defect on the STRA6 gene.
• Midline field defects: Congenital problems that occur along the vertical axis of the body. Defects can involve the brain, spine, heart, genitals and midline of the head and face.
• Milk poisoning: Milk poisoning is a condition where the body is too alkaline and the blood contains too much calcium. It can be caused by drinking large quantities of milk or using too many alkaline antacid remedies. High vitamin D intake can make the condition worse. The people most at risk of this condition tend to be older people (especially women) who are taking calcium supplements as well as calcium carbonate containing remedies to treat dyspepsia.
• Milk-Alkali syndrome: Milk-Alkali syndrome is a condition where the body is too alkaline and the blood contains too much calcium which results in impaired kidney function. It can be caused by drinking large quantities of milk or using too many alkaline antacid remedies. High vitamin D intake can make the condition worse. The people most at risk of this condition tend to be older people (especially women) who are taking calcium supplements as well as calcium carbonate containing remedies to treat dyspepsia.
• Miscarriage: Symptoms related to miscarriage or stillbirth.
• Mitochondrial DNA depletion syndrome: A group of conditions called mitochondrial disorders involving a reduced number of mitochondrial DNA in tissues rather than defective mitochondrial DNA. The disorders generally involve neurological symptoms which can occur during infancy or childhood. Symptoms will vary depending on the specific order involved.
• Mixed asthma: Mixed asthma is a type of asthma that can be caused by an exposure to an allergen as well as other intrinsic triggers such as exposure to cold air or cigarette smoke. Mixed asthma involves constriction and inflammation of the airways that may or may not involve an allergic reaction.
• Mixed granulocytic asthma: Mixed granulocytic asthma is a type of asthma that is characterized by increased levels of eosinophils and neutrophils (types of white blood cell) in the airways. Asthma involves constriction and inflammation of the airways which makes breathing difficult. The severity of symptoms is variable.
• Moccasin snake poisoning: The Moccasin snake is a poisonous snake found mainly in America and Asia. Moccasin snakes include the copperhead, cottonmouth and the Siberian, Central Asian and Malayan pit vipers. They are considered less venomous than rattlesnakes The snake venom contains toxins which affect the blood and tissues rather than the nervous system. Children tend to suffer more severe symptoms due to their smaller body size. Rapid swelling of the skin around the site of the bite is a sign of a more severe poisoning.
• Mohave Rattle snake poisoning: The Mohave rattle snake is a poisonous snake found mainly in Mexico and south-western areas of the US. The type of venom in Mohave snakes varies amongst species. Those with Type A venom tend to affect the nervous system whereas those with Type B venom primarily affect the blood and tissues. Type A tends to be more toxic than type B. Children tend to suffer more severe symptoms due to their smaller body size.
• Monkshood poisoning: Monkshood is a poisonous plant with distinctive flowers. The perennial plant is native to Europe but is also grown in parts of the US and is sometimes used as a medicinal herb.
• Monosomy 1p36: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as heart problems, mental retardation, developmental delay, facial dysmorphism and short stature. The range and severity of symptoms is variable with some cases being relatively mild.
• Monosomy 8q21 q22: A very rare chromosomal disorder where a portion of chromosome 8q is missing resulting in various abnormalities.
• Morphine allergy: Taking morphine (a painkiller) can cause an allergic response in some people however this is considered rare. It involves the body's immune system overreacting to the drug. The type and severity of symptoms can vary considerable though skin symptoms are the most common allergic response to drugs.
• Morphine overdose: Morphine is a highly addictive drug used to treat pain. Excessive doses of the drug can result in various symptoms and even death in severe cases.
• Morse-Rawnsley-Sargent syndrome: A very rare syndrome characterized mainly by abnormal brain development and reduced fetal movement.
• Mort d'amour syndrome: A term used to describe a condition where death occurs during sexual intercourse. It can occur in patients with a preexisting coronary disease.
• Mountain andromeda poisoning: The Mountain Andromeda is an evergreen flowering shrub bearing elongated clusters of white flowers. The leaves and flower nectar contain a chemical called andromedotoxin which is highly toxic. Ingesting the leaves or nectar can result in death as the plant is considered highly toxic.
• Mouser rodenticide poisoning: Mouser is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Mucolipidoses: A group of inherited metabolic disorders involving the accumulation of carbohydrates (glycosaminoglycans) and lipids within the tissues of the body due to a deficiencies or abnormal action of various lysosomal enzymes. This abnormal accumulation of carbohydrates and lipids within cells causes them to be damaged which often results in symptoms such as mental retardation and skeletal deformities. Symptoms may become apparent at birth or during childhood or adolescence. Premature death can occur in severe cases. There is a vast array of symptoms that can occur depending on the specific disorder involved.
• Mucopolysaccharidosis 1: A rare inherited condition caused by the absence of certain lysosomal enzymes which are needed to break down mucopolysaccharides. Without these enzymes, mucopolysaccharides build up in various body organs and tissues which causes harmful effects. There are three subtypes of the condition: Hurler, Scheie and Hurler-Scheie with Hurler being the most severe and Scheie the mildest.
• Mucormycosis: An infectious disease caused by fungus from the order Mucorales which is normally found in the soil and in decaying plant matter. Transmission is usually through the inhalation of spores. It is generally harmless to healthy individuals but can cause infection in patients who are immunocompromised or who have a serious chronic illness such as uncontrolled diabetes. Symptoms and severity can vary considerable depending on the part of the body the infection occurs in - gastrointestinal tract, skin, lungs, central nervous system, eye orbit and the paranasal sinuses.
• Muller-Barth-Menger syndrome: A rare disorder characterized by brain malformations, seizures, excessive hairiness and overlapping fingers.
• Mullerian derivatives - lymphangiectasia - polydactyly: A rare syndrome characterized by extra fingers, Mullerian duct remnants and lymphangiectasia.
• Multicystic renal dysplasia, bilateral: A rare congenital disorder where multiple cysts develop in the kidneys which affects their ability to function normally. The condition is results in death prior to or within weeks of birth.
• Multifocal ventricular premature beats: A form of abnormal heart rhythm that occurs in otherwise healthy individuals. Exertion or high emotions may trigger a fainting episode.
• Multiminicore disease (MmD): A rare congenital muscle disorder involving weakness and wasting of skeletal muscles. The term minicore comes from the small core structures that occur in the muscle tissue. There are four subgroups of the disorder: classic form (rigid spine syndrome), progressive form with hand involvement, antenatal form with arthrogryposis multiplex congenital and the ophthalmoplegic form. The rate of progression and severity of symptoms is variable.
• Multiple Sclerosis: Autoimmune attack on spinal nerves causing diverse and varying neural problems.
• Multiple Skeletal abnormalities with Anterior Segment Anomalies of the Eye and Early Lethality: A rare condition characterized by various skeletal and eye abnormalities and early death. The parents of the children reported with the condition are believed to be related.
• Multiple congenital anomalies - mental retardation - growth failure and cleft lip/ palate: A very rare syndrome characterized mainly by mental retardation, growth failure, cleft lip, cleft palate and various other abnormalities.
• Multiple joint dislocations - metaphyseal dysplasia: A rare disorder characterized by multiple joint dislocations and abnormal bone development as well as various other anomalies.
• Multiple pterygium syndrome: A very rare disorder characterized by webbing of various parts of the body, contractures, short stature, fusion of neck vertebrae and facial anomalies.
• Multiple pterygium syndrome lethal type: A rare syndrome characterized by skin, muscle and skeletal anomalies and fetal death.
• Mungan syndrome: A recessively inherited disorder characterized by heart abnormalities and gastrointestinal abnormalities. Death has occurred in some cases during the late teenage years.
• Muscle phosphoglycerate kinase deficiency: An inherited genetic muscle disease where an enzyme deficiency (phosphoglycerate kinase) affects the normal processes that convert carbohydrates from food into energy.
• Muscular Dystrophy - Late Onset: Muscle weakness and wasting that occurs later in life. The severity is variable with severe cases involving wheelchair confinement and death can occur if the heart muscle becomes involved. Progression may be slow or rapid. Slow progressing cases can result in a normal life span.
• Mustard tree poisoning: The mustard tree is found in various parts of America and contains nicotine. Ingestion of the plant can cause various symptoms. The leaves of the plant is sometimes smoked for its effects but it can result in death.
• Mycoplasma pneumoniae: Bacterial respiratory infection
• Myelodysplastic syndromes: A group of syndromes characterized by a disruption in the production of blood cells. Often the bone marrow increases production of various blood cells but because many of them are defective, they are destroyed before the reach the blood stream.
• Myocarditis: A condition which is characterized by inflammation of the muscles of the heart
• Myoclonus progressive epilepsy of Unverricht and Lundborg: A rare genetic brain disease characterized by convulsions which become progressively worse. Modern treatment can have a big effect on the prognosis.
• Myopathy, X-linked with postural muscle atrophy: An inherited, adult-onset muscle disease where the postural muscles become progressively weak and wasted while other muscles become enlarged. During early adulthood, patients tend to have an athletic build and muscle symptoms tend to start during the fourth decade of life. Death usually occurred between the ages of 40 and 75 years of age due to involvement of the heart.
• Myopathy, congenital nonprogressive with Moebius and Robin sequences: A rare inherited disorder characterized by nonprogressive muscle weakness from birth as well as the Moebius (congenital facial palsy with impaired ability to move eyes) and Pierre Robin sequence (underdeveloped jaw, cleft soft palate, abnormal tongue position).
• NADH CoQ reductase, deficiency of: A rare genetic defect where an enzyme deficiency (NADH CoQ) disrupts cellular processes and causes various organic acid disorders. Any of a variety of the components of the enzyme may be missing or defective and hence the clinical presentation and severity may vary. Presentation may range from infantile death to various disorders neurodegenerative disorders such as Leigh's disease, Parkinson's disease and cardiomyopathy.
• NEMO mutation with immunodeficiency: A very rare form of immunodeficiency caused by a mutation of the NEMO (NF-kappa-B essential modulator) gene on chromosome Xq28. The immunodeficiency causes sufferers to develop pus-forming bacterial infections early in life and as they get older, they tend to become susceptible to mycobacterial infections.
• Naked brimcap poisoning: Naked brimcap is a brown mushroom which becomes slimy when wet and is covered in thin hairs. The mushroom is often found growing in the wild in the US. This mushroom is poisonous and can lead to death if sufficient quantities are eaten. They are considered less toxic if cooked. This mushroom is unusual in that some people are able to eat them if they are cooked for a long time without any ill effect and can then develop a condition called immune hemolysis (where the body's immune system attacks it's own red blood cells).
• Narcotic addiction: An uncontrollable desire to use narcotics on a regular basis. The drug may be used as a therapeutic medication for various conditions but it's use is also frequently abused. Examples of narcotic drugs include heroin, morphine, Demerol and codeine. Frequent use leads to an increased tolerance to the drug so higher and higher doses are required to achieve the desired euphoric feeling.
• Nasal decongestant-induced hypertension: Nasal decongestant-induced hypertension is high blood pressure caused by taking nasal decongestants. Patients with an existing history of hypertension may suffer further blood pressure increases while taking amphetamines and this can be serious. Severity of symptoms varies amongst patients depending on their susceptibility, underlying health and duration of nasal decongestant use.
• Nasopharyngeal carcinoma: A malignant cancer that occurs in the nasopharynx area which is the upper part of the throat. Often there are no symptoms until the cancer has metastasized to other parts of the body such as the neck.
• Natal teeth, intestinal pseudoobstruction and patent ductus: A very rare syndrome characterized mainly by poor immunity, intestinal and heart problems and the premature eruption of primary teeth.
• Naxos disease: A very rare syndrome characterized mainly by heart disease and woolly hair.
• Necrobacillosis: A form of bacterial blood infection caused by Fusobacterium necrophorum which can occur as a complication of throat infections. The infection is potentially fatal and can cause the development of abscesses in various parts of the body including the brain and lungs .
• Necrotizing enterocolitis: A rare disease that is tends to occur in premature infants and involves inflammation and destruction of gastrointestinal tissue. It usually occurs within weeks of birth - often after the start of milk feeding. The condition can be extremely serious and even fatal.
• Necrotizing fasciitis: A severe, progressive skin infection which causes progressive destruction of skin and underlying tissue. It is caused by certain bacteria and has a high mortality rate.
• Nemaline myopathy 2: A very rare inherited muscle disorder and is characterized by muscle weakness caused by the presence of nemaline rods in the muscle tissue which affects its function. There are at least 7 different subtypes of nemaline myopathy, each with a different genetic defect. The severity of the symptoms may vary greatly even among patients within a particular subtype of the disorder. Type 2 is caused by a defect on the nebulin gene on chromosome 2q22.
• Nemaline myopathy 3: A very rare inherited muscle disorder and is characterized by muscle weakness caused by the presence of nemaline rods in the muscle tissue which affects its function. There are at least 7 different subtypes of nemaline myopathy, each with a different genetic defect. The severity of the symptoms may vary greatly even among patients within a particular subtype of the disorder. Type 3 is caused by a defect on the alpha-actin gene.
• Neonatal bacterial meningitis: Bacterial meningitis that occurs in an infant under 3 months of age. Bacterial meningitis is a bacterial brain infection.
• Neonatal hepatitis: A rare life-threatening condition where iron accumulates in the liver of the fetus and produces severe symptoms after birth. Death is common during the fetal or infant stage.
• Neonatal mortality: The neonatal death rate
• Nephrogenic Fibrosing Dermopathy: A rare disorder characterized by thickening and hardening of the skin as well as other symptoms. The course of the disease may be mild or aggressive and occurs in patients with underlying disorders kidney disease.
• Nephronophthisis - hepatic fibrosis: A rare syndrome characterized by progressive destruction of kidney tissue (nephronophthisis) which occurs from birth and results in kidney failure and liver fibrosis.
• Nephrotic syndrome ocular anomalies: A rare disorder characterized by the association of particular eye anomalies with kidney disease. Kidney failure occurs before or soon after birth with death occurring within months of birth.
• Nerve sheath neoplasm: Tumors that develop from the protective sheath surrounding nerves. There are two types of nerve sheath tumors: schwannomas and neurofibromas. They most often occur around the spinal cord. Symptoms are determined by the size and exact location of the tumor.
• Neurocutaneous melanosis: A rare genetic disorder characterized by melanosis of the skin and central nervous system deterioration.
• Neurocysticercosis: Brain/CNS infection with the tapeworm Cysticercosis
• Neurodegenerative syndrome, X-linked, Bertini type: A very rare neurodegenerative disorder characterized mainly by reduced muscle tone, ataxia, recurring bronchopulmonary infections and psychomotor deficit. The disorder is X-linked and thus only males suffer the full extent of the symptoms whereas female carriers may be asymptomatic or have only mild symptoms.
• Neurodegenerative syndrome, X-linked, Hamel type: A very rare neurodegenerative disorder characterized mainly by mental retardation, blindness, convulsions, spasticity and early death. The disorder is X-linked and thus only males suffer the full extent of the symptoms whereas female carriers may be asymptomatic or have only mild symptoms.
• Neuroectodermal tumor, primitive: A very rare type of tumor that occurs in children under the age of ten. It is very aggressive and has a poor prognosis with less than half of patients surviving. The tumor originates from primitive nerve cells in the brain (CNS PNET) or other parts of the body (peripheral PNET). CNS tumors can be further divided into infratentorial tumors (e.g. medulloblastoma) or supratentorial tumors. The tumors usually cause no symptoms in the early stages and the symptoms that do develop will vary depending on the exact location and size of the tumor.
• Neuroectodermal tumors primitive: A type of brain tumor that consists of small round cells and is believed to originate from primitive nerve cells in the brain. Symptoms are determined by the exact location of the tumor.
• Neuroendocrine carcinoma of the cervix: A rare form of cervical cancer which tends to be quite aggressive.
• Neurofibromatosis, familial intestinal: A rare type of familial tumor that arises from intestinal nerves.
• Neurofibrosarcoma: A rare type of tumor that develops from cells that provide a protective layer around nerves (nerve sheath). Symptoms are determined by the size and location of the tumor. The arms and legs are most commonly affected.
• Neuronal intranuclear inclusion disease: A very rare syndrome characterized mainly by muscle and nerve degeneration.
• Neurotoxicity syndromes: Altered nervous system functioning caused by exposure to certain chemicals (manmade or natural) that affect the nervous system - essentially it is the poisoning of the nervous system. Examples of toxic compounds that may cause neurotoxicity include lead, certain solvents and pesticides. Symptoms may occur immediately or gradually over a period of time.
• Neutrophilic asthma: Neutrophilic asthma is a type of asthma that is characterized by increased levels of neutrophils (a type of white blood cell) in the airways. Asthma involves constriction and inflammation of the airways which makes breathing difficult. The severity of symptoms is variable. This type of asthma is usually driven by such things as pollution and viral infections rather than exposure to an allergen.
• Nijmegen Breakage Syndrome: A very rare syndrome characterized mainly by a small head, reduced immunity and increased risk of cancer. There are a wide range of other abnormalities and symptoms that can occur.
• Nocturnal asthma: Nocturnal asthma is a type of asthma that tends to only produce symptoms at night. Asthma involves constriction and inflammation of the airways which makes breathing difficult. The severity of symptoms is variable. Factors such as airconditioning, gastroesophageal reflux and sleeping in a reclining positing may increase the incidence of this form of asthma in susceptible patients.
• Nodular melanoma: Nodular melanoma is the most aggressive form of melanoma. It grows in vertical direction from the outset and grows very fast (months). Nodular melanoma has no known precursor. It is a small black, or if amelanotic, pink nodule that simply enlarges. The lesions tend to bleed.
• Non functioning pancreatic endocrine tumor: A tumor of the pancreas that does not result in an increased hormone production but can cause symptoms when the tumor becomes big enough to push against other structures. The tumor may be malignant or benign.
• Non-Food Allergy - Africanized honeybee: An Africanized honeybee allergy is an adverse reaction by the body's immune system to an Africanized honeybee sting. Multiple stings increase the risk of a severe reaction or death. The body's immune system produces immunoglobulin E (IgE - an antibody) and histamine in response to contact with the allergen. The specific symptoms that can result can vary amongst patients.
• Non-Food Allergy - Ant: An ant bite allergy is an adverse reaction by the body's immune system to an ant bite. Multiple bites increase the risk of a severe reaction or death. Certain ants pose more of an allergy risk than others e.g. red fire ant. The specific symptoms that can result can vary amongst patients.
• Non-Food Allergy - Black fire ant: A black fire ant bite allergy is an adverse reaction by the body's immune system to a black fire ant bite. Multiple bites increase the risk of a severe reaction or death. The specific symptoms that can result can vary amongst patients.
• Non-Food Allergy - Bumblebee: A Bumblebee allergy is an adverse reaction by the body's immune system to a Bumblebee sting. Multiple stings increase the risk of a severe reaction or death. The body's immune system produces immunoglobulin E (IgE - an antibody) and histamine in response to contact with the allergen. The specific symptoms that can result can vary amongst patients.
• Non-Food Allergy - Hornet: A hornet allergy is an adverse reaction by the body's immune system to a hornet sting. Multiple stings increase the risk of a severe reaction or death. The body's immune system produces immunoglobulin E (IgE - an antibody) and histamine in response to contact with the allergen. The specific symptoms that can result can vary amongst patients.
• Non-Food Allergy - Red fire ant: A red fire ant bite allergy is an adverse reaction by the body's immune system to a red fire ant bite. Multiple bites increase the risk of a severe reaction or death. The specific symptoms that can result can vary amongst patients.
• Non-Food Allergy - Tropical fire ant: A tropical fire ant bite allergy is an adverse reaction by the body's immune system to a tropical fire ant bite. Multiple bites increase the risk of a severe reaction or death. The specific symptoms that can result can vary amongst patients.
• Non-Food Allergy - Yellow jacket Wasp: A yellow jacket allergy is an adverse reaction by the body's immune system to a yellow jacket wasp sting. Multiple stings increase the risk of a severe reaction or death. The body's immune system produces immunoglobulin E (IgE - an antibody) and histamine in response to contact with the allergen. The specific symptoms that can result can vary amongst patients.
• Non-Food Allergy - honey bee: A honey bee allergy is an adverse reaction by the body's immune system to a honey bee sting. Multiple stings increase the risk of a severe reaction or death. The body's immune system produces immunoglobulin E (IgE - an antibody) and histamine in response to contact with the allergen. The specific symptoms that can result can vary amongst patients.
• Non-Food Allergy - scorpion: A scorpion allergy is an adverse reaction by the body's immune system to a scorpion sting. Multiple stings increase the risk of a severe reaction or death. The specific symptoms that can result can vary amongst patients.
• Non-Food Allergy - wasp: A wasp allergy is an adverse reaction by the body's immune system to a wasp sting. Multiple stings increase the risk of a severe reaction or death. The body's immune system produces immunoglobulin E (IgE - an antibody) and histamine in response to contact with the allergen. The specific symptoms that can result can vary amongst patients.
• Non-Small Cell Lung Cancer: It is any type of lung cancer other than small cell carcinoma (SCLC). As a class, NSCLCs are relatively insensitive to chemotherapy, compared to small cell carcinoma
• Non-allergic asthma: Non-allergic asthma is a type of asthma that is not triggered by exposure to an allergen. Non-allergic asthma involves constriction and inflammation of the airways that can be caused by such things as exercise, cold air, cigarette smoke and inhalation of chemicals.
• Non-atopic asthma: Non-atopic asthma refers to inflammation and constriction of the airways that is not caused by exposure to an allergen. The severity of symptoms is variable.
• Non-diarrheal (D-) HUS syndrome: A rare condition characterized by hemolytic anemia, thrombocytopenia and kidney failure that is not associated with diarrhea which means that it is not a result of bacterial gastroenteritis. This form of hemolytic uremic syndrome may be caused by kidney transplants, certain drugs (cyclosporine, tacrolimus, cytotoxic drugs), pregnancy, malignancy, HIV, non-diarrheal bacterial infections, immunological conditions or it may be inherited or in some cases there is no obvious cause (idiopathic).
• Non-ketotic hyperglycinemia: A rare disorder of amino acid metabolism where glycine and proline are unable to be metabolized properly due to defects in the glycine cleavage system.
• Novacaine drug allergy: Taking Novacaine (local anesthetic often used in dentistry) can cause an allergic response in some people however this is considered rare. It involves the body's immune system overreacting to the drug. The type and severity of symptoms can vary considerable though skin symptoms are the most common allergic response to drugs.
• Novak syndrome: A very rare syndrome characterized mainly underdeveloped lungs and by an abnormal opening in the area of the larynx, trachea and esophagus.
• Nyssen-Van Bogaert-Meyer syndrome: A very rare genetic disorder characterized by progressive degeneration of the central nervous system.
• Obesity - colitis - hypothyroidism - cardiac hypertrophy - developmental delay: A rare syndrome characterized by obesity, colitis, hypothyroidism, enlarged heart and developmental delay. The two reported cases involved maternal HELLP syndrome during pregnancy. Both infants died within months of birth.
• Obesity associated asthma: Obesity associated asthma refers to inflammation and constriction of the airways that is associated with obesity. The severity of symptoms is variable.
• Obstructive sleep apnea: Obstructive sleep apnea (OSA) syndrome is characterized by episodic upper airway obstruction that occurs during sleep.
• Occupational asthma: Occupational asthma refers to inflammation and constriction of the airways that occurs in a workplace setting. There is a wide range of chemicals and other airway irritants that are used in a workplace settings and can result in inhalation exposure that can produce asthma symptoms. The severity of symptoms is variable. Occupational exposures can also exacerbate existing asthma symptoms.
• Occupational lead exposure - ammunition production: Exposure to lead can occur in people employed as ammunition makers if adequate precautions are not taken. Lead exposure can cause elevated levels of lead in the blood which in turn can cause various symptoms depending on the severity and duration of the exposure.
• Occupational lead exposure - battery manufacturing: Exposure to lead can occur in people employed in the battery manufacturing industry if adequate precautions are not taken. Lead exposure can cause elevated levels of lead in the blood which in turn can cause various symptoms depending on the severity and duration of the exposure.
• Occupational lead exposure - brass foundry: Exposure to lead can occur in people employed in the brass foundry industry if adequate precautions are not taken. Lead exposure can cause elevated levels of lead in the blood which in turn can cause various symptoms depending on the severity and duration of the exposure.
• Occupational lead exposure - ceramic production: Exposure to lead can occur in people employed in the ceramic production industry if adequate precautions are not taken. Lead exposure can cause elevated levels of lead in the blood which in turn can cause various symptoms depending on the severity and duration of the exposure.
• Occupational lead exposure - explosives production: Exposure to lead can occur in people employed in the explosives production industry if adequate precautions are not taken. Lead exposure can cause elevated levels of lead in the blood which in turn can cause various symptoms depending on the severity and duration of the exposure.
• Occupational lead exposure - furniture refinishing: Exposure to lead can occur in people employed in the furniture refinishing industry if adequate precautions are not taken. Lead exposure can cause elevated levels of lead in the blood which in turn can cause various symptoms depending on the severity and duration of the exposure.
• Occupational lead exposure - lead glass factury: Exposure to lead can occur in people employed in lead glass factories if adequate precautions are not taken. Lead exposure can cause elevated levels of lead in the blood which in turn can cause various symptoms depending on the severity and duration of the exposure.
• Occupational lead exposure - lead mine: Exposure to lead can occur in people employed in lead mines if adequate precautions are not taken. Lead exposure can cause elevated levels of lead in the blood which in turn can cause various symptoms depending on the severity and duration of the exposure.
• Occupational lead exposure - lead smelting: Exposure to lead can occur in people employed in the lead smelting industry if adequate precautions are not taken. Lead exposure can cause elevated levels of lead in the blood which in turn can cause various symptoms depending on the severity and duration of the exposure.
• Occupational lead exposure - painter: Exposure to lead can occur in painters if adequate precautions are not taken. Lead exposure can cause elevated levels of lead in the blood which in turn can cause various symptoms depending on the severity and duration of the exposure.
• Occupational lead exposure - pottery making: Exposure to lead can occur in people involved in pottery making if adequate precautions are not taken. Lead exposure can cause elevated levels of lead in the blood which in turn can cause various symptoms depending on the severity and duration of the exposure.
• Occupational lead exposure - radiator repair: Exposure to lead can occur in people employed in the radiator repair industry. The soldering required to repair the radiator can lead to the lead exposure if adequate precautions are not taken. Lead exposure can cause elevated levels of lead in the blood which in turn can cause various symptoms depending on the severity and duration of the exposure.
• Occupational lead exposure - ship building: Exposure to lead can occur in people employed in the ship building industry if adequate precautions are not taken. Lead exposure can cause elevated levels of lead in the blood which in turn can cause various symptoms depending on the severity and duration of the exposure.
• Occupational lead exposure - ship repairing: Exposure to lead can occur in people employed in the ship repairing industry if adequate precautions are not taken. Lead exposure can cause elevated levels of lead in the blood which in turn can cause various symptoms depending on the severity and duration of the exposure.
• Occupational lead exposure - smelting: Exposure to lead can occur in people employed in the smelting industry if adequate precautions are not taken. Lead exposure can cause elevated levels of lead in the blood which in turn can cause various symptoms depending on the severity and duration of the exposure.
• Octopus poisoning: Octopus bites are quite rare but octopus such as the blue-ringed octopus can deliver quite a venomous bite.
• Ocular melanoma: A type of cancer that develops in the eye. The cancer develops from pigment-producing cells called melanocytes. This cancer becomes more common with increasing age.
• Oculo cerebro acral syndrome: A very rare syndrome characterized mainly by eye, brain, ear and limb abnormalities.
• Oesophagostomiasis: A parasitic intestinal infection caused by a nematode called Oesophagostomum bifurcum. The parasite commonly infects monkeys, goats, cattle, sheep and pigs. The infection is relatively rare in humans but is most commonly found in northern Togo and Ghana. Transmission usually occurs through oral contact with contaminated soil.
• Oleander poisoning: The oleander is a flowering shrub or small tree which bears clusters of flowers. The plant originated from Eurasia and is often used as an ornamental plant. The plant contains chemicals (cardiac glycosides: nerioside, oleandroside; saponins) which are very toxic if ingested. The plant is considered highly toxic and can result in death if sufficient quantities are eaten. The toxicity within a species can vary depending on the season. As little as seven leaves have been reported to cause poisoning symptoms. Poisoning can occur from inhaling smoke from burning oleander leaves.
• Oligohydramnios: An abnormally small amount of amniotic fluid surrounding the fetus during pregnancy.
• Ollivier syndrome: Symptoms associated with a crush injury usually involving the chest or abdomen. The condition is observed in people being trampled in a crowd stampede.
• Omsk hemorrhagic fever: A hemorrhagic fever caused by a virus. A serious outbreak occurred in Omsk and hence the name. Transmission occurs through tick bites. The infection has two phases: the first acute phase involves symptoms such as fever, rash and muscle pain and the second phase occurs after a week or two and involves the central nervous system (e.g. delirium, convulsions).
• Opioid addiction: An uncontrollable desire to use opioids on a regular basis. Opioids may may be prescribed by a physician for the purpose of pain relief but patients may become physically dependent on the drug and continue to obsessively use it even after the condition it was prescribed for has resolved. In other cases, opioid addiction results from the illicit use of the drug for recreational purposes. Frequent use leads to an increased tolerance to the drug so higher and higher doses are required to achieve the desired euphoric feeling. Examples of opioids includes morphine, heroin, oxycodone and fentanyl.
• Opitz G Syndrome: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: one is inherited in a X-linked manner and the other is inherited in an autosomal dominant manner. Females with the X-linked form of the condition tend to have few symptoms and often only have wide set eyes.
• Opitz G/BBB Syndrome: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: one is inherited in a X-linked manner and the other is inherited in an autosomal dominant manner. Females with the X-linked form of the condition tend to have few symptoms and often only have wide set eyes.
• Opitz G/BBB Syndrome, Type II: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: Type I inherited in a X-linked manner and type II is inherited in an autosomal dominant manner.
• Opitz G/BBB Syndrome, X-linked: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: type I is inherited in a X-linked manner and type II is inherited in an autosomal dominant manner. Females with type I tend to have few if any symptoms - often the only symptom is wide-set eyes.
• Opitz G/BBB Syndrome, type I: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: type I is inherited in a X-linked manner and type II is inherited in an autosomal dominant manner.
• Opitz G/BBB syndrome, Autosomal dominant: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: type I is inherited in a X-linked manner and type II is inherited in an autosomal dominant manner.
• Opitz syndrome , X-linked: A congenital disorder characterized by distinctive facial features, genital abnormalities, esophageal defect and difficulty swallowing. Males are more severely affected than females.
• Opium addiction: An uncontrollable desire to use opium on a regular basis. Opium may may be prescribed by a physician for the purpose of pain relief but patients may become physically dependent on the drug and continue to obsessively use it even after the condition it was prescribed for has resolved. In other cases, opium addiction results from the illicit use of the drug for recreational purposes. Frequent use leads to an increased tolerance to the drug so higher and higher doses are required to achieve the desired euphoric feeling.
• Opium overdose: Opium is an illegal recreational drug. Excessive doses of the drug can result in various symptoms and even death in severe cases.
• Optic pathway glioma: A type of tumor that arises in the optic nerve which sends messages from the eye to the brain. These tumors tend to occur mainly in children under the age of 10. The tumor may affect the hormone center of the brain and hence can affect such things as growth and weight.
• Opticoacoustic nerve atrophy dementia: A rare genetic disorder characterized by degeneration of the optic nerve (causing impaired vision), deafness due to nerve damage and dementia due to calcification of the central nervous system. Death usually results by about the age of 40 with extensive calcification of all parts of the nervous system.
• Oral facial digital syndrome, type 4: A rare inherited disorder characterized by facial, digital and oral abnormalities. Type IV is differentiated from the other types by the presence of severe shinbone deformity.
• Oral squamous cell carcinoma: A type of cancer that develops in the mouth. Smoking and alcohol can increase the risk of this cancer. The cancer can develop in any part of the mouth including the tonsils, pharynx, tongue, lip and palate. The tumor tends to invade and tissue nearby.
• Orbital lymphoma: A tumor that develops in the soft tissue of the eye socket and can push against the eye causing problems with vision and eye movement.
• Oriental Hornet poisoning: The Oriental hornet can deliver a venomous sting which can result in serious and even life-threatening symptoms. Allergies to the venom are also a possible life-threatening consequence. Multiple stings increase the severity of symptoms.
• Ornithine Transcarbamylase Deficiency: A rare metabolic disorder where a deficiency of the enzyme ornithine transcarbamylase means that nitrogen isn't removed from the body and builds up in the blood in the form of ammonia.
• Ornithine transcarbamylase (OTC) Deficiency: A rare metabolic disorder where a deficiency of the enzyme ornithine transcarbamylase means that nitrogen isn't removed from the body and builds up in the blood in the form of ammonia.
• Ossification anomalies - psychomotor development delay: A rare syndrome characterized by poor mineralization of skull bones, reduced muscle tone, thin long bones and various other problems.
• Osteopetrosis with neuroaxonal dysplasia, infantile form: A rare disorder characterized by abnormally increased bone density as old bone is not resorbed and replaced with new bone as well as nervous system problems.
• Osteopetrosis, autosomal recessive 2: A rare disorder characterized primarily by increased bone density as old bone is not resorbed and replaced with new bone - is also known as marble bone disease. This form is relatively mild with survival possible for a couple of decades in some cases.
• Osteopetrosis, autosomal recessive 4: A rare disorder characterized primarily by increased bone density as old bone is not resorbed and replaced with new bone - is also known as marble bone disease. The malignant infantile form is the most severe form of this disorder and death usually occurs in the first decade of life.
• Otocephaly syndrome: A rare, fatal disorder characterized mainly by the absence of a jaw as well as other abnormalities. The disorder usually involves other severe birth defects. Death occurs as a result of the inability to breath properly due to the structural defects.
• Ovarian germ cell malignant tumor: Development of cancer in the tissue of the eggs (germ cells) in the ovaries.
• Ovarian germ cell tumor: Development of cancer in the tissue of the eggs (germ cells) in the ovaries.
• Oxycontin addiction: Oxycontin is a commonly prescribed pain killer which is recognized as carrying a high risk of addiction. Initial use of the drug may be to control chronic pain but patients may find themselves increasingly dependent on the drug and unable to stop its use. Other cases of addiction may occur when people deliberately and illegally misuse Oxycontin as a recreational drug.
• Oxycontin overdose: Oxycontin is a prescription drug mainly used to treat pain. Excessive doses of the drug can result in various symptoms and even death in severe cases.
• PFIC: A rare inherited condition where bile is unable to drain from the liver where it builds up and causes progressive liver damage. End-stage liver disease usually occurs before adulthood. There are three different subtypes of the disorder, each with a different genetic origin of the defect.
• Pain killer addiction: An uncontrollable desire to use pain-relieving medication on a regular basis. Pain killers are often prescribed for the treatment of sleeping problems but chronic use can lead to dependence on the drug. Frequent use leads to an increased tolerance to the drug so higher and higher doses are required to achieve the desired euphoric feeling.
• Palytoxin poisoning: Palytoxin is a marine toxin found in sea anemones and certain crabs and fish (e.g. triggerfish). The toxin is extremely potent and death is common in patients who ingest contaminated fish.
• Pancreatic abscess: A localized pus-filled cavity (abscess) in the pancreas which usually occurs after pancreatitis. Death can occur if the abscess is not drained.
• Pancreatic beta cell agenesis with neonatal diabetes mellitus: A very rare syndrome characterized mainly by abnormal development of the pancreas resulting in infant diabetes mellitus. The insulin-producing beta cells are absent from birth.
• Pancreatic cancer, adult: Cancer that develops in the tissues of the pancreas. The pancreas produces digestive juices and certain hormones such as insulin that regulate sugar levels in the body and tumors can in some cases causes excessive hormone secretion.
• Pancreatic carcinoma, familial: Cancer (malignant) that develops in the pancreas and tends to run in families. The pancreas produces digestive juices and certain hormones such as insulin that regulate sugar levels in the body.
• Pancreatic islet cell tumors (non-functioning tumor): A tumor that arises from the pancreatic islet cells and may involve cells that produce excess pancreatic hormones.
• Papillary renal cell carcinoma: A type of kidney tumor characterized by the development of finger-like projections in at least some of the tumor. It can be inherited in a familial pattern or occur sporadically.
• Paraganglioma: A rare, usually benign tumor most often found in the abdomen, chest, head and neck areas. The tumor develops from glomus cells which are located along blood vessels involved in automatic body activities such as regulation of blood pressure and blood flow. Symptoms may vary depending on the exact location of the tumor.
• Paralytic shellfish poisoning: Rare food poisoning from eating contaminated shellfish
• Paranasal sinus cancer, adult: Cancer that develops in the paranasal sinus which are spaces behind the cheeks and nose.
• Paraquat lung: A condition caused by inhalation of paraquat (herbicide) which causes lung damage such as stiffening (fibrosis) of lung tissue and hence breathing problems.
• Parkinson disease, juvenile, autosomal recessive: A rare form of Parkinson disease that tends to occur by the age of 40 and is inherited in a recessive manner. Symptoms tend to be more severe during the day rather than the night.
• Paroxetine toxicity: The toxic reaction of the body to the substance, possibly via allergic reaction or overdose.
• Paroxysmal ventricular fibrillation: A rare condition where the heart has an abnormal rhythm for no detectable reason. The condition can lead to fainting attacks and even sudden death in an otherwise healthy individual.
• Parrotfish poisoning (Palytoxin): Palytoxin is a marine toxin found in some parrotfish from the Philippines and Singapore region. The toxin is extremely potent and death is common in patients who ingest contaminated parrotfish.
• Partial Trisomy 18 Syndrome: A rare genetic chromosomal syndrome where the child has an extra third copy of only part of chromosome 18 in the body's cells. It is a less severe form of Edwards syndrome - the most severe form involves and extra copy of the whole of chromosome 18 in all of the body's cells. The severity of the condition is highly variable depending on how many of the body's cells are involved and how much of the chromosome is involved.
• Parvovirus antenatal infection: Fetal infection with human parvovirus B19 - serious abnormalities rarely occur.
• Patau syndrome: A chromosomal disorder where there are three number 13 chromosomes as opposed to the normal two. The condition causes mental retardation and heart, kidney and scalp defects. Survival rate is very poor.
• Paucigranulocytic asthma: Paucigranulocytic asthma is a type of asthma that is characterized by normal levels of eosinophils and neutrophils (types of white blood cell) in the airways. Asthma involves constriction and inflammation of the airways which makes breathing difficult. The severity of symptoms is variable.
• Pay-loo-ah-induced lead poisoning: Pay-loo-ah is a folk remedy used mainly by the Hmong people from Loas to treat fever and rash. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Peach seed poisoning: Peach seeds contain a chemical called amygdalin which breaks down into cyanide in the human body. The toxic chemicals are not released if the seed remains intact and therefore poisoning usually occurs if the seeds are crushed and eaten. Accidental ingestion is very unusual. Most parts of the peach plant contain the toxic chemical with the highest concentration in young leaves.
• Peanut allergies: A hypersensitive state that is due to exposure to an allergen contained in peanuts
• Pearson's anemia: Pearson's anemia is a rare progressive condition characterized by abnormal pancreatic functioning and sideroblastic anemia. Diagnosis usually occurs within the first 7 years of life and death in infancy is common.
• Pearson's marrow-pancreas syndrome: A rare condition characterized by abnormal functioning of the bone marrow, liver, kidneys and pancreas. Infant death is common.
• Pediatric AIDS: Pediatric AIDS is an immune system disease in infants or children caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AIDS-related condition such as opportunistic infections. Symptoms in children are similar to those of an adult but their susceptibility to various AIDS-related conditions varies e.g. children are less susceptible to Kaposi sarcoma, taxoplasmosis and cryptococcosis than adults.
• Pemphigus Vulgaris: A severe autoimmune skin disease characterized by blistering of the skin including the mucous membranes inside the mouth and esophagus.
• Pemphigus and fogo selvagem: An autoimmune skin disease characterized by skin blisters and a burning sensation. It is endemic particularly in Brazil but may also occur in other countries.
• Pemphigus paraneoplastic: A rare type of autoimmune skin blistering disease which affects the skin and/or mucous membranes and occurs in patients with cancer.
• Penicillin allergy: Taking penicillin (a type of antibiotic) can cause an allergic response in some people. It involves the body's immune system overreacting to the drug. The type and severity of symptoms can vary considerable though skin symptoms are the most common allergic response to drugs. Penicillin allergy is one of the more common types of drug allergies.
• Penicillin-induced Immune Hemolytic Anemia: Penicillin-induced immune hemolytic anemia is a condition where use of a medication called Penicillin triggers the body's immune system to destroy it's own red blood cells which results in anemia.
• Percocet overdose: Percocet is a prescription drug used to treat pain. Excessive doses of the drug can result in various symptoms and even death in severe cases.
• Perinatal-lethal Gaucher disease: A disorder caused by a deficiency of an enzyme called glucocerebrosidase. The foetal form is one of several forms of Gaucher disease and is the rarest. The fetal form causes death before birth or soon after.
• Peripartum cardiomyopathy: A rare condition involving weakening of the heart in the final stages of pregnancy or within five months of giving birth. The cause of the condition is unknown and patients usually have no history of heart disease. The breathing difficulty associated with the condition is often ignored as a normal symptom in the late stages of pregnancy which increases the risk of potentially fatal complications developing.
• Peripheral neuroectodermal tumor: A type of tumor that consists of small round cells and occurs in bone or soft tissue in the extremities of the body such as the arms, legs, pelvis or chest wall. Symptoms are determined by the location of the tumor. The tumor may be malignant or benign.
• Peritonitis: Inflammation of the peritoneum.
• Pernettya poisoning: Pernettya is a shrubby plant found mainly in the southern parts of the world. It is often utilized as an ornamental shrub. The leaves, berries and flower nectar contain a chemical called andromedotoxin which can cause symptoms if eaten. Serious cases of poisoning can result in death.
• Peroxisomal bifunctional enzyme deficiency: A rare disorder involving abnormal steroid metabolism due to an enzyme 17-beta-hydroxysteroid dehydrogenase 4) deficiency. The symptoms which make the condition appear very similar to another condition called neonatal adrenoleukodystrophy.
• Peroxisomal defects: A group of metabolic disorders caused by genetic anomalies resulting in dysfunctional peroxisomes. Peroxisomes are found in cells in the body and are involved in functions such as metabolizing certain fatty acids and producing bile acid. Examples of condition involving peroxisomal defects includes Zellweger syndrome and adrenoleukodystrophy. The range and severity of symptoms vary greatly depending on the particular condition involved.
• Pfeiffer syndrome Type 2: A rare genetic disorder characterized by premature joining of certain skull bones during development which has an impact on the shape of the head and face. Features include craniofacial and cardiovascular malformations with death often occurring early.
• Pfeiffer syndrome Type 3: A rare genetic disorder characterized by premature joining of certain skull bones during development which has an impact on the shape of the head and face. Features include craniofacial abnormalities, cardiovascular malformations and early death is common.
• Pheochromocytoma as part of Neurofibromatosis: A tumor that develops in the part of the adrenal gland called the medulla which produces adrenalin and noradrenaline. This tumor is often associated with a condition called neurofibromatosis. The tumor affects automatic body activities such as regulating breathing rate and heartbeat.
• Pheochromocytoma-induced hypertension: Pheochromocytoma-induced hypertension is high blood pressure caused by an adrenal gland tumor. The high blood pressure often responds poorly to the usual medications. Death can result in severe cases.
• Phosgene oxime - inhalation exposure: Phosgen oxime has no useful purpose but may be manufactured for use as a chemical weapon. The chemical is poisonous and exposure can occur through ingestion, inhalation and absorption through the skin. Inhalation causes mainly respiratory symptoms. The severity of symptoms will vary depending on the extent and duration of the exposure.
• Phosgene oxime - skin exposure: Phosgen oxime has no useful purpose but may be manufactured for use as a chemical weapon. The chemical is poisonous and exposure can occur through ingestion, inhalation and absorption through the skin. The chemical can penetrate clothing and the severity of symptoms will vary depending on the extent and duration of the exposure.
• Phyllodes tumor of the prostate: A rare type of tumor that occurs in the prostate. The tumor is usually benign but may become malignant and tends to have a leaf-like appearance.
• Pindone rodenticide poisoning: Pindone is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Pineal Teratoma: A type of brain tumor that occurs mainly in the pineal region of the brain.
• Pinealoma: A slow-growing type of brain tumor that occurs in the pineal gland. The pineal gland produces a hormone called melatonin which is involved in regulating sleep patterns.
• Pineoblastoma, adult: A rare type of highly malignant brain tumor that usually occurs in children. The tumor develops in the pineal region of the brain.
• Pituitary cancer, childhood: Cancer (malignant) of the pituitary gland in children. The pituitary gland produces various hormones and some pituitary tumors (functioning tumors) can affect the secretion of one or more of these hormones resulting in a range of symptoms depending on the exact location of the tumor. Some pituitary tumors do not affect hormone production (nonfunctioning tumors).
• Pituitary tumors, adult: A benign or cancer tumor that develops in the tissue of the pituitary gland in adults. The pituitary gland produces various hormones and some pituitary tumors (functioning tumors) can affect the secretion of one or more of these hormones resulting in a range of symptoms depending on the exact location of the tumor. Some pituitary tumors do not affect hormone production (nonfunctioning tumors).
• Placenta conditions: Any condition that affects the placenta
• Plague: Any epidemic disease with a high death rate.
• Plant poisoning - Acetylandromedol: Acetylandromedol is a chemical found naturally in plants from the Ericaceae family which includes rhodendrons. Human poisoning can occur through eating honey made from pollen and nectar from these flowers or from eating other parts of the plant. The severity of symptoms may vary from mild to life-threatening depending on the amount consumed.
• Plant poisoning - Aconitum: Aconitum is a toxin found in certain plants from the Aconitum genus e.g. Monkshood. It is a highly poisonous neurotoxin that affects the heart and other parts of the body. It can cause serious symptoms and even death in severe cases. The toxin can be absorbed through the skin to some degree.
• Plant poisoning - Amygdalin: Amygdalin is a chemical found naturally in various plants e.g. stone fruit kernels and raw almonds. Eating these parts of the plant that contain the chemical can cause symptoms of cyanide poisoning as the amygdalin is converted to cyanide by the digestive process. Obviously, the concentration of the chemical varies amongst species of plant and often, significant quantities are needed to produce symptoms. Nevertheless, severe poisoning can result in death. Amygdalin is believed by some to inhibit cancers but there has been no conclusive proof of this.
• Plant poisoning - Andromedotoxin: Andromedotoxin is a toxin found naturally in plants such as aloe vera, senna, rhubarb and Cascara buckthorn. The main symptoms are gastrointestinal which can range in severity depending on the amount consumed. Severe cases can result in kidney damage and gastrointestinal bleeding.
• Plant poisoning - Calcium oxalate crystals: Calcium oxalate crystals is a chemical found naturally in plants such as dumb cane and rhubarb leaves. The amount of calcium oxalate crystals varies amongst species of plant. The crystals are quite sharp and abrasive and ingestion of plants containing them can cause abrasive and irritation injuries. Eating large amounts can cause kidney and liver damage and even death in serious cases.
• Plant poisoning - Conline: Conline is a toxin found naturally in plants such as aloe vera, senna, rhubarb and Cascara buckthorn. The main symptoms are gastrointestinal which can range in severity depending on the amount consumed. Severe cases can result in kidney damage and gastrointestinal bleeding.
• Plant poisoning - Cyanogenic glycoside: Cyanogenic glycoside is a toxin found naturally in various plants e.g. cherries, plums, almonds, peaches, apricots, apples and cassava. The chemical is usually concentrated in the seeds, kernels or wilted leaves. Eating these parts of the plant that contain the chemical can cause symptoms of cyanide poisoning as the cyanogenic glycoside is converted to cyanide by the digestive process. Even chewing the leaves can result in conversion to cyanide due to the presence of digestive enzymes in the mouth. Obviously, the concentration of the chemical varies amongst species of plant and often, significant quantities are needed to produce symptoms. Nevertheless, severe poisoning can result in death.
• Plant poisoning - Cytisine: Cytisine is a chemical found naturally in plants from the Faboideae family e.g. Laburnum, Cytisus, Genista and Sophora. It tends to have an effect similar to nicotine.
• Plant poisoning - Euphorbiaceae: Euphorbiaceae is a family of flowering plants called spurges. They contain various chemicals (alkaloids, glycosides and diterpene ester) which can cause symptoms if ingested.
• Plant poisoning - Grayanotoxin: Grayanotoxin is a chemical found naturally in plants from the Ericaceae family which includes rhodendrons. Human poisoning can occur through eating honey made from pollen and nectar from these flowers or from eating other parts of the plant. The severity of symptoms may vary from mild to life-threatening depending on the amount consumed.
• Plant poisoning - Hydroquinone: Hydroquinone is a chemical metabolized by the human digestive system from a naturally occurring chemical called arbutin found in the leaves of plants such as blueberries, cranberries, bearberries and red whortleberries. The main symptoms are irritation of the gastrointestinal mucosa but severe poisoning can cause systemic symptoms.
• Plant poisoning - Indole alkaloids: Indole alkaloids are a group of chemicals found naturally in plants such as snakeroot and Madagascar periwinkle. Specific indole alkaloids from this group are vinblastine, reserpine and vincristine.
• Plant poisoning - Lantadene: Lantadene is a toxin found naturally in a plant called lantana camara. The chemical is toxic to the liver and can cause various symptoms if ingested. The green fruit and leaves are the most toxic parts of the plant.
• Plant poisoning - Rhodotoxin: Rhodotoxin is a chemical found naturally in rhodendrons. Human poisoning can occur through eating honey made from pollen and nectar from these flowers or from eating other parts of the plant. The severity of symptoms may vary from mild to life-threatening depending on the amount consumed.
• Plant poisoning - Tetranortriterpene: Tetranortriterpene is a toxin that occurs naturally in some plants (e.g. Chinaberry tree). It functions as a natural insect repellant but is toxic to the human nervous system. Ingesting plant parts with this chemical can cause poisoning symptoms.
• Plant poisoning - Toxalbumin: Toxalbumin is a toxin found naturally in plants such as the castor bean. The severity of symptoms depends on the particular species of plant involved and the amount consumed. For example the toxalbumin called ricin found in castor beans is extremely toxic.
• Plasmacytoma anaplastic: The malignant proliferation of plasma cells. The tumor can develop in bone and soft tissue and thus results in a range of symptoms depending on the exact location.
• Pleuropulmonary blastoma: A type of tumor that originates from precursor cells or blasts (immature or embryonic tissue) in the lungs or covering of the lungs.
• Plexosarcoma: A rare type of tumor that occurs in the gastrointestinal tract and retroperitoneum.
• Pneumocystosis: Infection of the lung by a fungal organism called pneumocystis Carinii. The organism is found readily in most environments but generally does not affect healthy individuals. It occurs almost exclusively in immunocompromised people such as AIDS sufferers or those undergoing chemotherapy.
• Pneumonia, Staphylococcal: Inflammation of the lungs and bronchioles caused by the Staphylococcal bacteria. The condition is not common and often occurs as a complication of influenza or other viral respiratory infections. This form of pneumonia is considered serious and up to a third of cases can result in death.
• Pneumonic plague: Severe flea-borne bacterial disease affecting the lungs
• Po Ying Tan-induced lead poisoning: Po Ying Tan is a folk remedy used mainly by Chinese people to treat minor childhood complaints. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Poison hemlock poisoning: Poison hemlock is a herbaceous plant which has a relatively large taproot and clusters of small white flowers. The plant if often found growing in the wild as a weed. The plant contains various alkaloid chemicals which can cause symptoms if eaten. Severe cases of poisoning can result in death.
• Polar bear poisoning: Polar bears are often used as a food source by the arctic inhabitants. Eating the liver and kidneys of the polar bear is believed to result in a Vitamin A overdose which can cause serious symptoms and even death in extreme cases. Eating more than 200 grams of Polar bear liver can result in human death however death is considered rare.
• Polychondritis: A serious, progressive, episodic condition characterized by inflammation and degeneration of cartilage in the body. The duration and severity of the episodes can vary.
• Polycystic kidney disease, infantile type: Severe form of polycystic kidney disease which is a genetic kidney disease. Symptoms develop very early in life and may even be present during the fetal stage.
• Polydactyly cleft lip palate psychomotor retardation: A very rare syndrome described in a small inbred group of families and characterized by bifid toes, extra big fingers, cleft lip or palate and psychomotor retardation. There were various other symptoms that were variably present.
• Polydactyly visceral anomalies cleft lip palate: A rare syndrome characterized mainly by the association of extra digits, cleft lip and/or palate and visceral anomalies. Various other abnormalities may also be present.
• Polyembryoma: An aggressive type of tumor that develops from germ cells. It occurs mainly in the ovaries but sometimes in the testes.
• Polymorphic catecholergic ventricular tachycardia: A very rare disorder involving an abnormal heart rhythm in an apparently otherwise normal heart. By the second decade of life, half of the sufferers will die.
• Polymorphous low-grade adenocarcinoma: A rare type of tumor of the salivary gland that occurs mainly on the roof of the mouth.
• Polyneuropathy - Ophthalmoplegia - Leukoencehalopathy - Intestinal Pseudo-Obstruction: A rare genetic disorder which affects a number of body systems and manifests results in symptoms such as droopy eyelids, progressive eye muscle weakness, gastrointestinal dysmotility, brain disease, thin body, peripheral neuropathy and muscle disease.
• Polyradiculoneuropathy: An inflammatory disorder that affects the peripheral nerves and the spinal nerve roots. The onset and progression of the disease is variable with severe cases resulting in premature death. The condition is chronic and progressive but periodic relapses can occur.
• Polysyndactyly - cardiac malformation: A very rare syndrome characterized mainly by an extra toe, webbed fingers and heart malformations.
• Polysyndactyly overgrowth syndrome: A very rare syndrome reported in one infant and characterized by the association of multiple webbed digits with an overly large body size.
• Pontocerebellar Hypoplasia Type 2B: A rare inherited condition where the brainstem and part of the brain (cerebellum) is abnormally small. Type 2B differs from other types with respect to the location of the genetic defect.
• Pontocerebellar Hypoplasia Type 2C: A rare inherited condition where the brainstem and part of the brain (cerebellum) is abnormally small. Type 2C differs from other types with respect to the location of the genetic defect.
• Pontocerebellar Hypoplasia Type 6: A rare inherited condition where the brainstem and part of the brain (cerebellum) is abnormally small.
• Pontocerebellar hypoplasia with infantile spinal muscular atrophy: A rare, recessively inherited disorder characterized by an abnormally small brain and brainstem which manifests as a small head and mental retardation. The disorder is lethal with death usually occurring within the first year. The brain progressively degenerates.
• Pontoneocerebellar Hypoplasi: A very rare disorder where a part of the brain fails to develop normally during the fetal stage. Some of the functions of this part of the brain include coordination, initiation and timing of movements and cognition.
• Pontoneocerebellar Hypoplasia: A very rare disorder where a part of the brain fails to develop normally during the fetal stage. Some of the functions of this part of the brain include coordination, initiation and timing of movements and cognition.
• Popliteal pterygium syndrome, lethal type: A rare lethal condition characterized by webbing of skin as well as various other physical and mental abnormalities.
• Post-vaccinial encephalitis: Post-vaccinial encephalitis is a brain infection that occurs after a smallpox vaccination.
• Posterior valve, urethra: A congenital defect where there is an abnormal membrane in the back of the male urethra which affects urine flow. The urine can flow back through the valve and cause problems for organs such as the urethra, bladder, ureters and even the kidneys. The severity of the condition is determined by the severity of the malformation. Severe defects can cause fetal death and mild defects may cause incontinence.
• Posthemorrhagic anemia: Posthemorrhagic anemia refers to a reduced number of red blood cells in the body due to bleeding.
• Postpartum Eclampsia: Postpartum eclampsia is the development of seizures or coma in pregnant women suffering from high blood pressure. Postpartum means that it soon after the delivery. Eclampsia is a serious condition which requires urgent medical treatment. Eclampsia may be associated with moderate as well as significant increases in blood pressure.
• Postpartum hemorrhage: Excessive bleeding after childbirth
• Postperfusion lung syndrome: A breathing complication that can occur within hours of heart surgery involving blood transfusions. Death is relatively common with this complication.
• Potter syndrome type 2: A term that describes the physical appearance that occurs when kidney disease results in a reduced volume of amniotic fluid. In type 2, one kidney is absent and the other is small and malformed.
• Potter syndrome type 4: The development of cystic kidneys due to obstruction of the kidneys or ureters for a long period of time.
• Powell-Buist-Stenzel syndrome: A rare syndrome inherited in a X-linked manner and characterized by diarrhea, endocrine disease and severe infections during infancy which lead to death. The condition is possibly due to an overactive immune system.
• Poxviridae disease: A group of infectious diseases that cause puss filled skin eruptions. Chicken pox and small pox are examples.
• Precocious myoclonic encephalopathy: An early-onset form of myoclonic seizures. It is caused by brain abnormalities due to such things as brain malformations and inborn errors of metabolism.
• Pregnancy toxemia /hypertension: Preeclampsia is the development of high blood pressure, excess protein in the urine and swelling during pregnancy. Hypertension is a serious health condition due to the fact that it often causes no symptoms until it is severe. The blood pressure usually returns to normal after delivery.
• Prescribed medication addiction: An uncontrollable desire to use prescribed medication in a manner or frequency not prescribed. Drugs such as painkillers are prescribed to treat such things as pain but patients may become physically dependent on the drug and continue to obsessively use it even after the condition it was prescribed for has resolved. Frequent use leads to an increased tolerance to the drug so higher and higher doses are required to achieve the desired euphoric feeling.
• Primary Autoimmune Hemolytic Anemia: Primary autoimmune hemolytic anemia is characterized by an abnormal immune system response. The body's immune system produces antibodies against the body's own red blood cells which leads to the destruction of red blood cells and hence anemia. The secondary form of the condition is the result of an underlying condition such as lupus or hepatitis whereas the primary form has no underlying condition.
• Primary Cold Autoimmune Hemolytic Anemia: Primary cold autoimmune hemolytic anemia is a condition where the body's immune system triggers the production of antibodies against the body's own red blood cells. The process occurs only when the patient is exposed to temperatures colder the average body temperature. The red cells are destroyed at an abnormally rapid rate which leads to anemia. The primary form of the condition means that there is no underlying condition. The condition may develop gradually or occur suddenly and cause serious symptoms.
• Primary Fallopian Tube Cancer: A cancer that originates in the fallopian tubes which form part of the female reproductive organs. This type of cancer is relatively uncommon.
• Primary amebic meningoencephalitis: A relatively rare but serious infectious disease caused by Naegleria fowleri which is a type of free-living amoeba that can be found in warm fresh water and damp soil. The incubation period is from a few days to a week.
• Primary cutaneous CD30-positive T-cell lymphoproliferative disorders: A form of primary T-cell lymphoma of the skin which is made up of CD30-positive anaplastic lymphoid cells. The condition generally has a very good prognosis with skin lesions usually regressing on their own though relapses can be frequent.
• Primary effusion lymphoma: A cancerous proliferation of lymphocytic B-cells caused by the human herpesvirus 8 (HHV-8, Kaposi's sarcoma-associated herpesvirus). It is more prevalent in immunodeficient people such as AIDS patients. The cancer tends to occur in the lining of body cavities such as the pericardium and peritoneum. The cancerous cells are detected in the fluid secreted from the lining of the cavity.
• Primary granulocytic sarcoma: A malignant tumor derived from immature white blood cells called myeloblasts. It can occur anywhere in the body but is most commonly found in bone, soft tissue, lymph nodes and skin. Symptoms will vary according to the location of the tumor.
• Primary hyperoxaluria type 2: A rare inherited inborn metabolic disorder characterized by excessive amounts of oxalate in the urine and deposits of oxalate in the kidneys which leads to progressive kidney failure. There are two subtypes of Oxalosis, each with a different origin for the genetic defect involved. Type 2 involves a deficiency of a liver enzyme called D-Glycerate Dehydrogenase. Type 2 tends to cause a milder disease than type 1 with better longterm outcomes.
• Primary malignant melanoma of the cervix: A form of cervical cancer where the tumor consists of pigment containing cells.
• Prinzmetal's variant angina: A rare disorder where the heart artery spasms which affects the blood flow to the heart and causes pain. The condition can occur with or without physical activity.
• Prion diseases: Various diseases caused by abnormal proteins (prions) in the brain.
• Privet poisoning: Privet is a shrubby plant which bears elongated clusters of small white flowers and black berries. The plant can be found growing in the wild or in gardens. The berries contain chemicals (ligustrin, syringin and other glycosides) which can cause symptoms if eaten. The plant is considered to be very toxic and death can result if sufficient quantities are eaten.
• Progressive Rubella Panencephalitis: A very rare complication of rubella infection where neurological symptoms develop following a congenital rubella infection and very rarely with childhood rubella. It is believed that the condition is the result of persistent rubella virus infection.
• Progressive Vaccinia: Progressive vaccinia is a serious complication of smallpox vaccination. The condition involves progressive death of tissue (necrosis) at the site of the vaccination. The condition is relatively rare but can result in death so prompt diagnosis and treatment is essential. People with AIDS, immunodeficiencies, cancer, receiving immunosuppressive therapies or have some other form of immune system defect are particularly susceptible to this complication.
• Progressive spinal muscular atrophy: A group of inherited motor neuron diseases involving progressive muscle weakness and wasting due to degeneration of motor neurons in the spinal cord. The severity of symptoms and survival varies depending on the particular form of the condition. Death can occur as early as infancy whereas some forms allow survival into adulthood.
• Properdin deficiency: A rare condition where an inherited deficiency of properdin (a blood plasma component) affects immunity. In particular, susceptibility to meningococcal disease is increased. There are three subtypes of the disorder: type I is a total deficiency, type II is a partial deficiency and type III is a deficiency due to abnormal function of the properdin.
• Properdin deficiency, type I: A rare condition where an inherited deficiency of properdin (a blood plasma component) affects immunity. In particular, susceptibility to meningococcal disease is increased. Type I is characterized by a total deficiency of properdin.
• Properdin deficiency, type II: A rare condition where an inherited deficiency of properdin (a blood plasma component) affects immunity. In particular, susceptibility to meningococcal disease is increased. Type II is characterized by a partial deficiency of properdin.
• Properdin deficiency, type III: A rare condition where an inherited deficiency of properdin (a blood plasma component) affects immunity. In particular, susceptibility to meningococcal disease is increased. Type III is characterized by the presence of dysfunctional properdin.
• Prostate cancer, familial: An inherited form of prostate cancer where cancer cells develop in the prostate tissue in males.
• Prostate cancer, hereditary, 1: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 1 is linked to a defect on chromosome 1q24-q25 and is inherited in a dominant manner.
• Prostate cancer, hereditary, 10: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 10 is linked to a defect on chromosome 8q24.
• Prostate cancer, hereditary, 11: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 11 is linked to a defect on chromosome 17p12.
• Prostate cancer, hereditary, 12: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 12 is linked to a defect on chromosome 2p15.
• Prostate cancer, hereditary, 13: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 13 is linked to a defect on chromosome 10q11.2.
• Prostate cancer, hereditary, 14: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 14 is linked to a defect on chromosome 11q13.
• Prostate cancer, hereditary, 15: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 15 is linked to a defect on chromosome 19q13.4.
• Prostate cancer, hereditary, 2: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 2 is linked to a defect on chromosome 17p11.
• Prostate cancer, hereditary, 3: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 3 is linked to a defect on chromosome 20q13.
• Prostate cancer, hereditary, 4: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 4 is linked to a defect on chromosome 7p11-q21.
• Prostate cancer, hereditary, 5: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 5 is linked to a defect on chromosome 3p26.
• Prostate cancer, hereditary, 6: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 6 is linked to a defect on chromosome 22q12.3.
• Prostate cancer, hereditary, 7: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 7 is linked to a defect on chromosome 15q12.
• Prostate cancer, hereditary, 8: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 8 is linked to a defect on chromosome 1q42.2-q43.
• Prostate cancer, hereditary, 9: Many forms of prostate cancer are due to inherited defect on a chromosome. Type 9 is linked to a defect on chromosome 17q21-q22.
• Prostate cancer, hereditary, X-linked 2: Many forms of prostate cancer are due to inherited defect on a chromosome. X-linked type 2 is linked to a defect on chromosome Xp11.22.
• Prostatic Stromal Proliferations of Uncertain Malignant Potential: A rare type of prostate tumor that may or may not be malignant.
• Proud-Levine-Carpenter syndrome: A very rare syndrome characterized mainly by abnormal brain development, a small head and genital abnormalities.
• Proximal spinal muscular atrophy: A rare group of muscle disorders which mainly affects the muscles closest to the trunk of the body. Muscles become progressively weak and wasted due to damage to motor neurons in the spinal cord and brainstem.
• Proximal tubulopathy - diabetes mellitus - cerebellar ataxia: A very rare syndrome characterized mainly by diabetes, movement disorder and kidney abnormality. Death often occurs during childhood.
• Pseudoglycogenosis II: A rare inherited disorder characterized by severe heart problems, varying degrees of muscle weakness and often mental retardation. Other symptoms such as mental retardation may also occur. The genetic anomaly manifests as a deficiency of a protein called LAMP-2 (Lysosomal-Associated Membrane Protein 2) which affects lysosomes.
• Psittacosis: An infectious disease caused by Chlamydia psittaci and transmitted mainly by infected birds but also by some mammals.
• Pterygium, Popliteal, lethal type: A rare lethal condition characterized by webbing of skin as well as various other physical and mental abnormalities.
• Pulmonary Alveolar Proteinosis: An abnormal condition where phospholipids and proteins are deposited in the alveoli of the lung. More prevalent in males with some patients having no symptoms and others having an unproductive cough and progressive dyspnea with exertion. The condition increases the risk of secondary infection. Also called alveolar proteinosis.
• Pulmonary Anthrax: Inhaled lung anthrax, most severe form of anthrax.
• Pulmonary alveolar microlithiasis: A rare form of lung disease characterized by tiny deposits of calcium phosphate throughout the alveoli in the lungs. The abnormal depositions may start at any age and the condition may progress very slowly with no symptoms for years or even decades. Cases which involve rapid progression or early onset are very uncommon.
• Pulmonary alveolar proteinosis, congenital: A rare lung disease where protein and fat molecules accumulate in the distant parts of the lungs and affect breathing.
• Pulmonary artery, isolated unilateral absence of (Isolated UAPA): A very rare malformation where either the right or left pulmonary artery is missing and there are no other heart abnormalities. The severity of the condition is variable with some infants being severely affected while others are asymptomatic for decades.
• Pulmonary atresia - intact ventricular septum: A very rare heart defect where the opening that allows blood to travel from the heart to the lung is narrowed or absent which impairs the body's ability to oxygenate blood. Death generally occurs without immediate medical attention.
• Pulmonary cystic lymphangiectasis: A rare congenital condition where the lungs fail to develop normally. The disorder is characterized by the presence of dilated lymph ducts throughout the lungs.
• Pulmonary embolism: The occurrence of an embolism which blocks blood vessels in the lungs
• Pulmonary haemosiderosis, primary: A rare condition characterized by anemia, coughing up blood and iron deposits in the lungs. The disorder is the result of recurring bleeding in the lungs which leads to a buildup of iron in the lungs. Symptoms may develop slowly or quickly and may become evident at any age.
• Pulmonary hypoplasia familial primary: A rare malformation where the lungs fail to develop properly. Death often occurs as a result.
• Pulmonary lymphangiectasia, congenital: A rare congenital condition where the lungs fail to develop normally. The disorder is characterized by the presence of dilated lymph ducts throughout the lungs.
• Pulmonary mucormycosis: An infectious disease caused by fungus from the order Mucorales which is normally found in the soil and in decaying plant matter. Transmission is usually through the inhalation of spores. It is generally harmless to healthy individuals but can cause infection in patients who are immunocompromised or who have a serious chronic illness such as uncontrolled diabetes. Symptoms and severity can vary considerable depending on the part of the body the infection occurs in - gastrointestinal tract, skin, lungs, central nervous system, eye orbit and the paranasal sinuses. Pulmonary mucormycosis involves infection of the lungs.
• Pulmonary surfactant protein B, deficiency of: A rare lung disease where protein and fat molecules accumulate in the distant parts of the lungs and affect breathing. The disease is called by a deficiency of a the lung surfactant protein B.
• Pulmonary valves agenesis: The total or partial absence of the pulmonary valve at birth. It is often associated with other malformations. Severity is variable.
• Pulmonary veno-occlusive disease: Any disease which causes a lung vein to become narrow or blocked. The pulmonary vein carries oxygenated blood from the lungs to various body tissues.
• Pulmonary zygomycosis: An infectious disease caused by fungus from the order Mucorales which is normally found in the soil and in decaying plant matter. Transmission is usually through the inhalation of spores. It is generally harmless to healthy individuals but can cause infection in patients who are immunocompromised or who have a serious chronic illness such as uncontrolled diabetes. Symptoms and severity can vary considerable depending on the part of the body the infection occurs in - gastrointestinal tract, skin, lungs, central nervous system, eye orbit and the paranasal sinuses. Pulmonary zygomycosis involves infection of the lungs.
• Pyknoachondrogenesis: A very rare lethal syndrome characterized mainly by abnormal skeletal growth as well as abnormal bone calcification.
• Pylephlebitis: A pus-producing inflammation of the wall of the portal vein that drains blood from the abdominal part of the gastrointestinal tract. The infection is often fatal. It usually occurs as a complication of abdominal or pelvic infections such as diverticulitis and appendicitis.
• Pyogenic pericarditis: The pericardium is the fibrous sac surrounding the heart. Infection can cause the pericardium to become inflamed and swollen and to produce pus. It may result from a ruptured esophagus, heart infection or from surgery involving the heart or chest cavity. The condition may be misdiagnosed as a heart attack and vice versa.
• Pyridoxamine 5-prime-phosphate oxidase deficiency: A metabolic disorder involving a deficiency of an enzyme called 5-prime-phosphate oxidase. Symptoms start soon after birth and involves seizures and other anomalies.
• Pyruvate dehydrogenase phosphatase deficiency: A genetic disease involving an enzyme deficiency which causes exercise intolerance and mild developmental delay. Symptoms are variable.
• Pyruvate kinase deficiency, liver type: An inherited deficiency of pyruvate kinase which causes varying degrees of hemolytic anemia.
• Pyruvate kinase deficiency, muscle type: An inherited deficiency of pyruvate kinase which causes varying degrees of hemolytic anemia.
• Q fever: A disease caused by Coxiella burnetti which causes fever, headache and muscle pain.
• Quinidine toxicity: The toxic reaction of the body to the substance, possibly via allergic reaction or overdose.
• Quinidine-induced Immune Hemolytic Anemia: Quinidine-induced immune hemolytic anemia is a condition where use of a medication called Methyldopa triggers the body's immune system to destroy it's own red blood cells which results in anemia.
• Rabies: An infectious disease that can affect any mammal including humans and is transmitted through the saliva of an infected animal. The infectious agent is the Neurotropic lyssavirus which affects the salivary gland and also causes neurological symptoms.
• Radiation induced angiosarcoma of the breast: A rare form of malignant breast tumor that occurs after exposure to radiation. Radiation is used to treat a variety of conditions such as cancer. The tumor can develop years or even decades after the exposure.
• Radiation related neoplasm: Tumors caused by exposure to radiation which is often used to treat various conditions. Usually the tumor develops many years or even decades after the exposure and the tumors tend to occur in the part of the body exposed to the radiation. The tumor can develop in virtually any part of the body and thus the symptoms are highly variable.
• Radio renal syndrome: A very rare syndrome characterized mainly by kidney, forearm and and thumb abnormalities.
• Raine syndrome: A very rare syndrome characterized mainly by increased bone density which ultimately results in death.
• Ratak Plus rodenticide poisoning: Ratak Plus is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Rattle snake poisoning: The Rattle snake is a poisonous snake found mainly in America. They are distinguished by a characteristic rattle at the tip of their tail.
• Rectal cancer: A growth or excessive proliferation of cells in the rectum which is the final portion of the digestive system before the anus. The growth may be benign or malignant.
• Rectosigmoid neoplasm: A tumor that originates in the upper rectal area or sigmoid colon. The tumor may be benign or cancerous.
• Red Imported Fire ant sting: The Red Imported Fire ant is found in parts of Australia and can cause allergic reactions in susceptible people. Some people have a relatively minor allergic response whereas other develop anaphylaxis which is a life-threatening allergic response which requires urgent medical attention. The ants have a venom gland attached to a stinger located in their tail region. Ants can sting more than once.
• Red buckeye poisoning: The red buckeye is a shrubby plant which bears a cluster of small red flowers and brown seeds with distinctive pale markings. The plant originated in the US. The seeds and leaves contain various chemicals (glycoside aesculin, saponin aescin and alkaloids) which can cause poisoning symptoms if eaten. The plant is considered very toxic and death can result in cases of severe poisoning.
• Refractory Celiac Disease: Refractory Celiac Disease is celiac disease that fails to respond to treatment which involves a gluten-free diet. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The condition is quite uncommon and often the resulting poor absorption of nutrients from the intestines leads to a poor prognosis.
• Refsum disease with increased pipecolic acidemia: A rare disorder involving all the clinical features of Refsum disease as well as high blood levels of L-pipecolic acid. Refsum disease is a metabolic disorder where a deficiency of phytanic acid alpha-hydroxylase results in a buildup of phytanic acid in the body which causes neurological disorders.
• Renal Cell Carcinoma 2: A genetic form of kidney cancer.
• Renal Cell Carcinoma 3: A dominantly inherited form of kidney cancer which is linked to chromosome 5q.
• Renal Cell Carcinoma 4: A genetic form of kidney cancer.
• Renal adysplasia dominant type: An inherited disorder of kidney development where either one kidney fails to develop normally, one kidney is absent, one kidney fails to develop normally and one kidney is absent or both kidneys are absent. Severity of the condition is highly variable: if there is one normal kidney the condition can be asymptomatic but if both kidneys are absent then the condition is lethal.
• Renal cancer, familial: A genetic form of kidney cancer that tends to run in families.
• Renal dysplasia - limb defects syndrome: A very rare syndrome characterized mainly by abnormal kidney development and various arm bone defects.
• Renal dysplasia diffuse autosomal recessive: A rare inherited kidney defect which is inherited in a recessive manner.
• Renal hypertension: Renovascular hypertension is high blood pressure resulting from narrowing or damage to kidney blood vessels which prevents the blood from flowing through the kidneys properly.
• Renal pelvis and ureter, transitional cell cancer: Cancer that develops in certain cells that make up the ureter and renal pelvis. The ureter is a tube that connects the kidney to the bladder and the renal pelvis is a part of the kidney. Transitional cells line the inside of the renal pelvis and the ureter.
• Renal segmental hypoplasia-induced Hypertension: Renal segmental hypoplasia-induced hypertension is high blood pressure resulting from either an abnormally developed kidney (birth defect) or from damage to the kidney resulting from vesicureteral reflux.
• Renal tubular transport disorders, inborn: Genetic defects in the transporters and channels along the kidney tubules that help to regulate body fluids as well as defects in the receptors and enzymes involved in the process. Examples of such disorders include nephrogenic diabetes insipidus and hereditary renal hypouricemia. Symptoms are determined by the exact nature of the disorder.
• Renal-genital-middle ear anomalies: A very rare syndrome characterized mainly by kidney, genital and middle ear abnormalities.
• Renovascular Hypertension: Renovascular hypertension is high blood pressure resulting from narrowing or damage to kidney blood vessels which prevents the blood from flowing through the kidneys properly.
• Resistant hypertension: Resistant hypertension is a form of high blood pressure that doesn't respond to treatment. Blood pressure remains high even when a combination of three drugs is used. It can be caused by such things a secondary hypertension, fluid retention or if the patient doesn't stick to the treatment plan.
• Respiratory Hypersensitivity: A hypersensitivity reaction that affects the breathing airways. Conditions such as asthma and hay fever are included in this term.
• Respiratory arrest: A term used to indicate cessation of breathing.
• Respiratory-Bronchiolitis-associated Interstitial Lung Disease: A relatively uncommon form of lung inflammation that has no apparent cause though the majority of patients have a history of smoking. Symptoms tend to develop over a period of six months to one and a half years.
• Reticuloendotheliosis: An inherited disorder of the reticuloendothelial system which is involved in destroying bacteria and other unwanted substances that enter the body.
• Retinopathy - anaemia- CNS anomalies: A very rare syndrome characterized mainly by disease of the eye retinas, anemia and central nervous system anomalies.
• Retroperitoneal liposarcoma: A rare, slow growing tumor that develops in the retroperitoneal cavity of the abdomen and tends to displace organs rather than destroy them. The tumor generally contains fat and soft tissue.
• Retropharyngeal abscess: The high mortality rate of retropharyngeal abscess is owing to its association with airway obstruction
• Rett's syndrome: Autism-like behavioral syndrome in infant girls
• Revesz Debuse syndrome: A very rare syndrome characterized mainly by disease of the eye retinas, anemia and central nervous system anomalies.
• Revesz Syndrome: A very rare syndrome characterized mainly by disease of the eye retinas, anemia and central nervous system anomalies.
• Reye's syndrome: is a potentially fatal disease that causes numerous detrimental effects to many organs, especially the brain and liver
• Rh Disease: A disease that can occur when the mother's blood is not compatible with the fetal blood i.e. when an Rh-negative mother had a Rh-positive child. If the baby's blood is exposed to the mother's blood (through placenta, abortion, miscarriage, amniocentesis) the mother's body becomes sensitized and develops antibodies the Rh-positive blood. In future pregnancies, the mother's antibodies can attack the red blood cells of the unborn baby resulting in hemolytic disease. The severity of the disease is variable and can range from mild fetal anemia to severe anemia and even fetal death.
• Rhabditida Infections: Infection with a parasitic worm from the order rhabditida. The symptoms are determined by the species involved.
• Rhabdoid tumor: An aggressive malignant tumor that occurs in children. Symptoms depend on the location of the tumor. The tumors often form in the kidneys and then tend to metastasize to the brain and sometimes the lungs.
• Rhabdomyosarcoma of the orbit: A type of tumor found around the eye area (orbit). The tumor is usually malignant.
• Rheumatic fever: An inflammatory disorder that can occur as a complication of untreated streptococcal bacterial infection such as strep throat or scarlet fever. The condition may affect the brain, skin, heart and joints.
• Rheumatic pericarditis: Inflammation and swelling of the pericardium (fibrous sac surrounding the heart) that occurs as a complication in people with rheumatism. Rheumatic pericarditis condition may be misdiagnosed as a heart attack and vice versa.
• Rhino-orbito-cerebral phycomycosis: Fungal infection of the brain, nose and brain. Infection usually occurs through inhalation of fungal spores and the condition is result in rapid death. It tends to occur in severely ill patients such as those suffering from severe diabetes, carcinomatosis, ketoacidosis or bacterial infections.
• Rhinocerebral mucormycosis: A rare opportunistic infection that tends to occur mainly in the brain and sinuses. The condition is usually fatal and generally only affects immunocompromised people such as patients with leukemia, lymphoma or those that have had organ transplants or chemotherapy. The infectious agent is saprophytic fungi.
• Rhinocerebral zygomycosis: An infectious disease caused by fungus from the orders Mucorales and Entomophthorales which are normally found in the soil and in decaying plant matter. The infection differs from mucormycosis which only involves the order Mucorales. Transmission is usually through the inhalation of spores. It is generally harmless to healthy individuals but can cause infection in patients who are immunocompromised or who have a serious chronic illness such as uncontrolled diabetes. Symptoms and severity can vary considerable depending on the part of the body the infection occurs in - gastrointestinal tract, skin, lungs, central nervous system, eye orbit and the paranasal sinuses. Rhinocerebral zygomycosis involves infection of the paranasal sinuses and the central nervous system.
• Rhodococcus equi: A rare form of bacterial infection that usually affects horses and foals but can cause infection mainly in immunocompromised people. Infection usually starts at the site of some sort of trauma. Symptoms and severity may vary considerably depending on the location and extent of the infection.
• Rickettsia siberica: An infectious disease caused by Rickettsia siberica and transmitted by ticks. The condition is endemic in central Asia and can be fatal in severe cases.
• Ringed seal poisoning: The Ringed seal is often used as a food source by the arctic inhabitants. Eating the liver of the ringed seal can result in a Vitamin A overdose which can cause serious symptoms and even death in extreme cases.
• Ritter syndrome: A rare infantile skin disorder involving severe redness, inflammation, blistering and peeling of skin and mucous membranes which can result from a variety of infections, malignancies and drugs.
• Roberts-SC Phocomelia: A rare genetic disorder characterized by limb deformities, midfacial defects and severe growth deficiency.
• Rocky Mountain spotted fever: A bacterial disease caused by Rickettsia rickettsii and transmitted by ticks. The condition causes fever and a characteristic rash and may be fatal in severe or untreated cases.
• Rodend rodenticide poisoning: Rodend is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Romano-Ward syndrome: A genetic heart disorder characterized by an abnormal heart rhythm (long Q-T interval) where the heart takes longer than normal to recharge between beats. The severity of the condition can vary.
• Rubella panencephalitis: A very rare complication of rubella infection where neurological symptoms develop following a congenital rubella infection and very rarely with childhood rubella. It is believed that the condition is the result of persistent rubella virus infection.
• Rubella virus antenatal infection: A rare disorder caused by exposure of the fetus to maternal rubella and resulting in a range of abnormalities and fetal death is also possible.
• Rudd-Klimek syndrome: A very rare syndrome characterized mainly by abnormal development of the tailbone with deformities of the urogenital area as well as other anomalies.
• Rueda-induced lead poisoning: Rueda is a lead-containing folk remedy used mainly by Chinese people to treat infant colic or to calm young children. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Rumination disorder: A chronic eating condition where the stomach contents are regurgitated, rechewed and swallowed again. It tends to occur predominantly in infants, young children and people with mental impairment but it can occur in otherwise healthy individuals. Sufferers often try to hide their condition for fear of being diagnosed as having bulimia. The condition is often misdiagnosed as gastroparesis or bulimia. The regurgitation can occur as soon as the food is swallowed or even up to an hour after finishing eating.
• Rumination disorder, infants: A condition where the stomach contents are regurgitated, rechewed and swallowed again.
• Rüdiger syndrome 2: A rare syndrome characterized by developmental failure, coarse face, underdeveloped ends of limbs and other abnormalities.
• SARS: Serious respiratory infection
• SCHAD Deficiency - formerly: A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activity prevents some fats being converted into energy. Symptoms tend to be exacerbated during fasting as during fasting, the body tries to rely more heavily on fats for energy. Fatty acids that are not completely metabolized due to the enzyme deficiency may build up in various organs and cause serious complications.
• SCHAD deficiency: A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Symptoms tend to be more severe in males who suffer progressive neurodegeneration whereas females tend to suffer mainly from developmental delay.
• Saal-Bulas syndrome: A very rare syndrome characterized mainly by lobster-like hands, diaphragmatic hernia and a brain abnormality.
• Sakamoto disease: An epidemic disease that tends to occur each year in Japan and affects infants and young children. Symptoms are similar to cholera and death can occur.
• Salicylate-sensitive asthma: Salicylate-sensitive asthma is a type of asthma that is triggered by salicylates which can be found in medications such as aspirin as well as many foods. Asthma involves constriction and inflammation of the airways which makes breathing difficult. The severity of symptoms is variable.
• Salmonella typhimurium infection: An infection caused by bacteria from the Salmonella genus which can result in gastroenteritis, fever or may be asymptomatic. Infection is caused by consuming contaminated food or drinks.
• Samson-Viljoen syndrome: A very rare syndrome characterized by small ears, abnormal chest wall and facial, lip and palate clefts.
• Santrinj-induced lead poisoning: Santrinj is a paint primer but is also used as a folk remedy mainly by Saudi Arabian people to treat teething and gum boils. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Saoot-induced lead poisoning: Saoot is a folk remedy used mainly by Middle Eastern people to treat digestive eye injuries, teething and to manage the umbilical stump in newborns. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Sarcoidosis: Rare autoimmune disease usually affecting the lungs.
• Sarcoma botryoides: An aggressive form of cancer that arises from embryonic muscle cells. The tumor resembles a bunch of grapes and tends to occur in the genitourinary tract. Common locations are the cervix, vagina and bladder and very rare cases can occur in the bile duct or the soft tissues of the head and neck. It occurs most often in female infants and young children. Symptoms will vary depending on the exact location of the tumor.
• Sardine poisoning (clupeotoxin): Some sardines contain toxins (Clupeotoxin) which can be poisonous to humans if eaten. Heat does not destroy the toxin and there is still uncertainty as to the origin of the toxin. The toxin appears to be present in higher concentrations in summer and is believed to be possible linked to the consumption of toxic food in its food web. The size and age of the sardines does not appear to be related to the toxicity. The sardines are found in coastal waters off Africa and the Caribbean, Indian and Pacific Oceans.
• Sarrouy disease: A disease characterized mainly by anemia, poor growth and enlarged liver and spleen. The disease usually ends with death.
• Scapuloperoneal syndrome, neurogenic type: An inherited disorder involving muscle wasting and weakness in the shoulder and lower leg. The legs are often affected first.
• Schaefer-Stein-Oshman syndrome: A rare disorder where excessive growth and abnormal hardening affects the head and facial bones.
• Schisis association: A medical term used to describe any condition involving two or more malformations of certain types. Malformations can include such things as oral clefts, neural tube defects, diaphragmatic hernias and omphaloceles.
• Schwannoma, malignant: A malignant tumor that develops from nerve sheath cells. Any nerve can be affected but it is most common on the sciatic, brachial and sacral plexus (leg, upper arm and lower back nerves). Symptoms are determined by the exact location of the tumor.
• Scleroderma, diffuse: A rare autoimmune connective tissue disease where the body attacks parts of the body and causes scarring and thickness of the tissue. In the diffuse form the the disorder, large areas of skin as well as organs are involved. Death can occur.
• Scleroderma, systemic: A rare autoimmune connective tissue disease where the body attacks parts of the body and causes scarring and thickness of the tissue. In the systemic form, the skin and organs are involved.
• Scleromyxedema: A rare connective tissue disorder which causes the skin to become progressively thick and hard. The severity of symptoms is variable with lungs and circulation affected in some patients. The degree of resulting disability, disfigurement and response to treatment is variable.
• Scotch broom poisoning: Scotch broom is a shrubby plant with tall straight stems giving it a broom-like appearance. The plant has bright yellow, pea-like flowers and a flat seed pod. The plant can be found growing in the wild and in the gardens. The seeds, stems and leaves of the plant contain a chemical called quinolixidine which can cause symptoms if eaten. Serious cases of poisoning can result in death.
• Sea snake poisoning: The Sea snake is a poisonous snake found in the warmer western parts of the Pacific and Indian Ocean. Sea snakes have scales but not gills or fins so they still need to go to the surface of the water to breathe. Sea snake venom is particularly poisonous but their bite fails to achieve any significant envenomation. The venom is toxic to the nervous system and muscles.
• Sea wasp poisoning: The sea wasp can deliver a serious sting and can be found in the waters of Northern Australia and the Philippines. Death can occur in as little as a few minutes if a person is severely stung.
• Sea wasp poisoning (Chiropsalmus quadrigatus): The Chiropsalmus quadrigatus jellyfish can deliver a serious sting and can be found in the waters of Northern Australia and the Philippines. Death can occur in as little as a few minutes if a person is severely stung.
• Sea wasp poisoning - Chironex fleckeri: The Chironex fleckeri jellyfish is one of the deadliest jellyfish in the world. It can deliver a serious sting and can be found mainly in the waters of Northern Australia and the Philippines. Death can occur in as little as a few minutes if a person is severely stung.
• Seasonal asthma: Seasonal asthma refers to inflammation and constriction of the airways that is triggered by the presence of airborne allergens such as pollen. This type of asthma tends to occur in a seasonal cycle in response to seasonal increases in levels of pollen and other airborne allergens in the air. The severity of symptoms is variable.
• Secernentea Infections: Infection with a type of parasitic nematode (worm). The symptoms are highly variable depending on where the worm migrates to through out the body and which particular species is involved. Some examples of nematodes are Wuchereria, Spirurina, Mansonella, Drucunculus, Loa and Ascaris.
• Seckel-like syndrome, Majoor-Krakauer type: A very rare syndrome characterized by numerous abnormalities including poor fetal growth, reduced amniotic fluid and heart, brain spleen and kidney anomalies.
• Secondary Autoimmune Hemolytic Anemia: Secondary autoimmune hemolytic anemia is characterized by an abnormal immune system response. The body's immune system produces antibodies against the body's own red blood cells which leads to the destruction of red blood cells and hence anemia. The secondary form of the condition is the result of an underlying condition such as lupus or hepatitis whereas the primary form has no underlying condition. The condition may develop gradually or occur suddenly and cause serious symptoms.
• Secondary Biliary Cirrhosis: Secondary biliary cirrhosis is a condition where the bile ducts are unable to transport bile effectively due to a secondary cause which results in blockage, inflammation, scarring or some other damage to the bile ducts. The condition may result from such things as congenital defect of the bile ducts (e.g. biliary atresia), cystic fibrosis, gallstones or a variety of other secondary conditions.
• Secondary Cold Autoimmune Hemolytic Anemia: Secondary cold autoimmune hemolytic anemia is a condition where the body's immune system triggers the production of antibodies against the body's own red blood cells. The process occurs only when the patient is exposed to temperatures colder the average body temperature. The red cells are destroyed at an abnormally rapid rate which leads to anemia. The secondary form of the condition means that it is the result of an underlying condition - it usually occurs after some sort of infection. The condition may develop gradually or occur suddenly and cause serious symptoms.
• Secondary Fallopian Tube Cancer: A cancer that originates in some other part of the body and metastasizes to the fallopian tubes which form part of the female reproductive organs. This type of cancer is relatively uncommon.
• Secondary Hypertension: Secondary hypertension is high blood pressure resulting from an underlying cause such as kidney disease. Hypertension is a serious health condition due to the fact that it often causes no symptoms until it is severe.
• Self-induced water intoxication and schizophrenic disorders syndrome: Excessive water intake associated with schizophrenia. The excessive water intake can lead to water intoxication and ultimately death. It is seen more commonly in schizophrenic patients than in the general population.
• Selye syndrome: A condition associated with prolonged extreme stress. The stressing agent may include such things as exposure to cold, starvation, death of someone close or work stress.
• Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis: A very rare syndrome characterized by progressive ataxia, eye muscle problems and a speech disorder (dysarthria).
• Sepsis Syndrome: A life-threatening condition that results from infection that has spread throughout the body.
• Septic abortion: An abortion associated with a uterine infection. The infection can occur during or just before or after an abortion. The infection can result from factors such as Chlamydia, IUD's or attempted abortion using infected tools.
• Septicemia: A systemic inflammatory response to an infection.
• Serine deficiency: A metabolic disorder caused by a deficiency of serine which results in various abnormalities.
• Serious digitalis intoxication: An adverse reaction to a drug called digitalis. The main symptoms involve heart and/or vision problems and death can occur in some cases.
• Serotoninergic syndrome: A disorder involves high levels of serotonin which can result from use of medications such as selective serotonin reuptake inhibitors.
• Serpentine fibula - polycystic kidney syndrome: A very rare syndrome characterized mainly by unusual s-shaped calf bone (fibula) as well as the development of numerous cysts in the kidneys.
• Serratia sepsis: Blood infection caused by bacteria from the Serratia genus. These bacteria are a rare cause of infection.
• Sertoli-leydig cell tumors: A rare form of ovarian cancer where excessive male sex hormones are produced by the cancerous cells.
• Severe dilated cardiomyopathy with or without myopathy: An inherited form of heart muscle disease where the heart ventricles become dilated which affects the hearts ability to function normally. The disorder is caused by the degeneration of the heart's conduction system due to a defect in the lamin A/C gene on chromosome 1q21. The heart disease may sometimes be associated with muscle disease which affects the quadricep muscles.
• Severe infantile axonal neuropathy: A rare disorder involving the early onset of severe neuropathy.
• Severe, refractory asthma: Severe refractory asthma is a type of asthma that is severe and difficult to treat. Asthma involves constriction and inflammation of the airways which makes breathing difficult.
• Sexual asphyxia syndrome: The practice of hanging oneself while masturbating to achieve greater sexual pleasure.
• Shaken Baby Syndrome: A condition caused by violent shaking of a baby.
• Sheep laurel poisoning: Sheep laurel is a small shrub which bears clusters of small white or pink flowers and encapsulated fruit. The plant contains chemicals (andromedotoxin and arbutin) which can cause various symptoms if ingested. The plant is considered to be very toxic and death can result if sufficient quantities are eaten.
• Shock: Physical and mental reaction to reduced circulation
• Shock, Cardiogenic: Shock is a life-threatening condition involving insufficient blood flow to the body tissues. Cardiogenic shock is caused by impaired heart function which means that blood is unable to be pumped effectively around the body.
• Shock, Distributive: Shock is a life-threatening condition involving insufficient blood flow to the body tissues. Distributive shock occurs when the blood vessels are dilated with affects blood volume and blood pressure within the vessels. Septic, neurogenic and anaphylactic shock are various forms of distributive shock.
• Shock, Endocrine: Shock is a life-threatening condition involving insufficient blood flow to the body tissues. Endocrine shock is caused by a disturbance in the endocrine (hormone producing) system. Some examples include severe cases of hypothyroidism, thyrotoxicosis and severe adrenal insufficiency.
• Shock, Hemorrhagic: Shock is a life-threatening condition involving insufficient blood flow to the body tissues. Hemorrhagic shock is caused by excessive bleeding which reduces the blood volume.
• Shock, Hypovolaemic: Shock is a life-threatening condition involving insufficient blood flow to the body tissues. Hypovolaemic shock is caused by a rapid fluid loss which reduces the blood volume.
• Shock, Neurogenic: Shock is a life-threatening condition involving insufficient blood flow to the body tissues. Neurogenic shock is caused problems with the nervous system.
• Shock, Obstructive: Shock is a life-threatening condition involving insufficient blood flow to the body tissues. Obstructive shock is caused by obstruction the blood flow. Causes include cardiac tamponade, pulmonary embolism and narrowing of the aortic artery.
• Shock, Septic: Shock is a life-threatening condition involving insufficient blood flow to the body tissues. Septic shock is caused by infection which affects large parts of the body. This form of shock results in death in about half of the cases.
• Shock, Traumatic: Shock is a life-threatening condition involving insufficient blood flow to the body tissues. Traumatic shock is caused by a serious injury or trauma to the body which affects the blood volume through one or more factors such as severe bleeding, heart damage and lung damage.
• Shock, anaphylactic: Shock is a life-threatening condition involving insufficient blood flow to the body tissues. Anaphylactic shock is a severe allergic response.
• Short QT syndrome: A very rare inherited condition where the heart muscle recharges between beats faster than normal which can result in various symptoms and even sudden death.
• Short QT syndrome 1: Short QT syndrome is a very rare genetic heart condition characterized by abnormalities in heart electrical signals - short QT interval. The severity of the condition is highly variable with some people suffering no noticeable symptoms whereas others have fainting spells or even die suddenly. There are three subtypes of the condition, each caused by a different genetic mutation. Type 1 is caused by a defect on chromosome 7q35-q36.
• Short QT syndrome 2: Short QT syndrome is a very rare genetic heart condition characterized by abnormalities in heart electrical signals - short QT interval. The severity of the condition is highly variable with some people suffering no noticeable symptoms whereas others have fainting spells or even die suddenly. There are three subtypes of the condition, each caused by a different genetic mutation. Type 2 is caused by a defect on chromosome 11p15.5.
• Short QT syndrome 3: Short QT syndrome is a very rare genetic heart condition characterized by abnormalities in heart electrical signals - short QT interval. The severity of the condition is highly variable with some people suffering no noticeable symptoms whereas others have fainting spells or even die suddenly. There are three subtypes of the condition, each caused by a different genetic mutation. Type 3 is caused by a defect on chromosome 17q23.1-q24.2.
• Short QT syndrome, familial: A very rare genetic heart condition characterized by abnormalities in heart electrical signals. The severity of the condition is highly variable with some people suffering no noticeable symptoms whereas others have fainting spells or even die suddenly.
• Short limb dwarf lethal, Mcalister Crane type: A very rare syndrome characterized mainly by short arms and legs and resulting in stillbirth or infant death.
• Short limb dwarfism, Al Gazali type: A very rare lethal disorder involving severe limb shortening and other skeletal deformities.
• Short ribs - craniosynostosis - polysyndactyly: A very rare syndrome characterized mainly by short ribs, premature fusion of skull bones and webbed fingers.
• Shy- Drager syndrome: also known as multiple system atrophy
• Silent asthma: Silent asthma is a type of asthma that occurs suddenly and is usually severe. The wheezing that usually precipitates and asthma attack is usually absent or very mild. Silent asthma involves rapid constriction and inflammation of the airways which makes breathing difficult.
• Silicosiderosis: A lung disorder caused by breathing in dust containing iron and silica.
• Silicosis: An occupation lung disease caused by breathing in silica dust.
• Silo unloader syndrome: An occupational lung disease that occurs in farm workers who go into a silo and breath in the nitrogen dioxide which are toxic to the body. Death can occur in some cases. Symptoms usually occur within a week of entering the silo.
• Simpson-Golabi-Behmel syndrome, type 1 (SGBS1): A rare genetic disorder characterized by accelerated growth, a peculiar face and other defects.
• Simpson-Golabi-Behmel syndrome, type 2: A rare genetic disorder characterized by hydrops fetalis and various other severe abnormalities. The condition usually results in death within two months of birth.
• Simvastatin - Teratogenic Agent: There is evidence to indicate that exposure to Simvastatin during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
• Sinonasal undifferentiated carcinoma: A rare but aggressive tumor that occurs in the nasal or sinus cavities.
• Sinus cancer: Cancer that originates from the mucosal tissue lining the sinus cavities or rarely from the bone itself.
• Sinus node disease and myopia: A very rare disorder characterized by nearsightedness
• Skeletal dysplasia, San Diego type: A very rare disorder characterized mainly by short limbs and flattened spinal vertebrae. Infants are stillborn or die soon after birth.
• Sketetal dysplasia coarse facies mental retardation: A rare skeletal disorder where the spine and long bones grow and develop abnormally as well as mental deterioration.
• Slap-cheek syndrome: Viral infection where children get rosy cheeks.
• Sleep apnea: A condition which is characterized by transient attacks of apnea that usually occur during ones sleep
• Sleeping pill addiction: An uncontrollable desire to use sleeping pills on a regular basis. Sleeping pills are often prescribed for the treatment of sleeping problems but chronic use can lead to dependence on the drug. Frequent use leads to an increased tolerance to the drug so higher and higher doses are required to achieve the desired euphoric feeling.
• Slickhead poisoning (clupeotoxin): Some slickhead contain toxins (Clupeotoxin) which can be poisonous to humans if eaten. Heat does not destroy the toxin and there is still uncertainty as to the origin of the toxin. The toxin appears to be present in higher concentrations in summer and is believed to be possible linked to the consumption of toxic food in its food web. The size and age of the slickhead does not appear to be related to the toxicity. The slickhead are found in coastal waters off Africa and the Caribbean, Indian and Pacific Oceans.
• Slowly Progressive Bokhoror: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. The slowly progressive form is the most common form and it has four phases: acute, recurrent-exacerbative, fully developed and terminal. Initial acute symptoms last for about 2 to 6 weeks.
• Slowly Progressive VE: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. . Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. The slowly progressive form is the most common form and it has four phases: acute, recurrent-exacerbative, fully developed and terminal. Initial acute symptoms last for about 2 to 6 weeks.
• Slowly Progressive Viliuisk Encephalitis: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. The slowly progressive form is the most common form and it has four phases: acute, recurrent-exacerbative, fully developed and terminal. Initial acute symptoms last for about 2 to 6 weeks.
• Slowly Progressive Viliuisk Encephalomyelitis: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. The slowly progressive form is the most common form and it has four phases: acute, recurrent-exacerbative, fully developed and terminal. Initial acute symptoms last for about 2 to 6 weeks.
• Slowly Progressive Vilyuisk Encephalitis: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. The slowly progressive form is the most common form and it has four phases: acute, recurrent-exacerbative, fully developed and terminal. Initial acute symptoms last for about 2 to 6 weeks.
• Slowly Progressive Vilyuisk Encephalomyelitis: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. The slowly progressive form is the most common form and it has four phases: acute, recurrent-exacerbative, fully developed and terminal. Initial acute symptoms last for about 2 to 6 weeks.
• Small Cell Lung Cancer: Small cell lung cancer is a cancer of the small cells which make up some of the lung tissue. It tends to be a more aggressive cancer than large cell lung cancer and can metastasize to other parts of the body. This type of cancer nearly always occurs in a people with a history of smoking.
• Small cell lung cancer, adult: Small cell lung cancer is a cancer of the lung tissue which is made up of small cells. It tends to be a more aggressive cancer than large cell lung cancer and can metastasize to other parts of the body.
• Small intestine cancer, adult: Cancer (malignant) that develops in the small intestine of adults.
• Smallpox: Dangerous virus now almost eliminated worldwide by vaccination.
• Smith-Lemli-Opitz syndrome, type 2: A rare birth disorder where an enzyme deficiency (7-dehydrocholesterol reductase) prevents cholesterol being metabolized properly. The condition causes a variety of physical abnormalities. Type II is a more severe form of the condition.
• Smoking: The smoking of cigarettes
• Smoking stools syndrome: Ingestion of yellow phosphorus (chemical found in many rodent poisons) which is toxic to the body. There is an initial phase involving symptoms such as vomiting and burning which is followed by an asymptomatic period (may last for weeks) and then symptoms caused by toxicity of various organs. Obviously symptoms and survival depend on the quantity of phosphorus involved.
• Smoldering adult T-Cell leukemia: A form of blood cancer affecting the T-cells which make up the body's immune system. The disease is caused by the HTLV-1 virus (human T-cell leukemia virus) which causes the proliferation of abnormal T-cells. The virus can be transmitted sexually and may lay dormant for decades. There are four subtypes: acute, chronic, lymphoma and smoldering. The acute and lymphoma subtypes have the poorest prognosis. The smoldering form tends to progress even slower than the chronic form and responds the best to treatment.
• Sodium Iodide - Teratogenic Agent: There is evidence to indicate that exposure to Sodium Iodide during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
• Solvent abuse: Solvent abuse is the use of various inhalants for the purpose of achieving a "high". They are often used as a cheap, readily available alternative to street drugs but they can cause serious damage to the body. Solvents include nail polish removers, paint thinners, gasoline, typing correction fluid and toxic markers. These solvents can be abused by sniffing them, spraying directly into the mouth, heating them and then inhaling them or injecting them directly into the body.
• Solvent addiction: Solvent addiction refers to the compulsive need to abuse solvents (e.g. sniffing them). Sufferers have withdrawal symptoms when attempting to stop the habit and feel unable to stop the habit despite knowing the harm it is causing their health. Solvents are very damaging to the body and can readily result permanent brain damage and even death. Death can occur through chronic use and in rare cases can occur after one session of use. Children and teenagers are particular at risk for this type of addiction - it is readily available and users feel it gains them greater acceptance from their peers. Solvents includes paint thinner, toxic markers, gasoline, cigarette lighter fluid, typing correction fluid and nail polish removers.
• Sphingolipidosis: A group of diseases involving the abnormal metabolism and storage of a substance called sphingolipid. Symptoms will vary depending on the disease. Examples of diseases from this group include gangliosidosis, Gaucher's disease and Niemann-Pick disease.
• Spinal cord neoplasm: A growth (tumor) that arises from the spinal cord. The tumor may be benign or malignant.
• Spinal muscular atrophy with respiratory distress 1: An inherited neuromuscular disease that causes progressive weakness in the arm and chest muscles leading to severe respiratory problems early in life. Sufferers are never able to sit independently and breathing problems progress rapidly with breathing assistance needed within the first five years.
• Spinal muscular atrophy, type I, with congenital bone fractures: A group of inherited motor neuron diseases involving progressive muscle weakness and wasting due to degeneration of motor neurons in the spinal cord. Bone fractures also occur in newborn infants.
• Spinocerebellar ataxia 10: A rare genetic disorder (chromosome 22q13 defect) characterized by gait ataxia and dysarthria (speech disorder). The severity of the condition is variable with some patients becoming wheelchair dependent.
• Spinocerebellar ataxia, X-linked, 2: A rare neurological disorder characterized mainly by ataxia, spasticity and early death.
• Spirochetes disease: Infection with a type of bacteria which is often found in mud, sewage and polluted water. Symptoms are determined by the species involved. Diseases caused by this bacteria include Treponema infection and borreliosis.
• Spleen neoplasm: A tumor that originates in the spleen.
• Splenic infarct: A relatively uncommon condition where a portion of spleen tissue dies due to a lack of sufficient blood supply to the affected tissue for any reason. An interruption in the blood supply can result from such things as emboli, thrombi, twisted blood vessels or blood pressure changes, trauma and blood disorders such as leukemia and abnormal blood coagulation. The severity of symptoms depends on the amount of spleen tissue involved.
• Spondylo-humero-femoral dysplasia: A rare genetic disorder characterized by bone formation abnormalities, short stature and early death.
• Spondylocostal dysostosis, autosomal recessive: A rare, recessively inherited syndrome characterized mainly by rib and spine abnormalities. The recessive form is more severe than the dominantly inherited form.
• Spondylocostal dysostosis, autosomal recessive 1: A rare, recessively inherited syndrome characterized mainly by rib and spine abnormalities. This form is severe and often results in infant death.
• Spondyloepimetaphyseal dysplasia joint laxity: A very rare syndrome characterized by abnormal bone growth involving severe scoliosis and loose joints.
• Spondyloepimetaphyseal dysplasia with joint laxity: A rare skeletal disorder where the spine and long bones grow and develop abnormally. Loose joints and severe curvature of the spine is also present. The condition is severe and death in the first couple of decades is common.
• Spondyloepimetaphyseal dysplasia, X linked with mental deterioration: A rare skeletal disorder where the spine and long bones grow and develop abnormally as well as mental deterioration.
• Spondylometaphyseal dysplasia, Sedaghatian type: A very rare syndrome characterized by abnormal bone development with short arms and flattened vertebrae. Death usually occurs within days of birth.
• Sporotrichosis - disseminated: A fungal infection caused by the fungus Sporothrix schenckii. Usually only the skin is infected but rarely it can spread to other parts of the body such as the bones and even the brain and central nervous system. The condition usually originates from fungal infection of a skin wound or from inhaling the fungus and can be life-threatening.
• Staggerbush poisoning: Staggerbush is a shrubby plant with small pink or white droopy flowers. The plant originated in the US. The leaves and flower nectar contain andromedotoxin which is very poisonous if eaten. Severe poisoning can result in death.
• Staphylococcal toxic shock syndrome: A very rare, potentially fatal infection caused by the bacterial toxins produced by Staphylococcus aureus or Streptococcus pyogenes. The condition is often associated with tampon use but can originate from other sources.
• Steinfeld syndrome: A very rare syndrome characterized by kidney abnormalities, single brain lobe and a heart defect.
• Stenotrophomonas maltophilia: A bacteria that is usually found in aquatic environments, is not very virulent and rarely infects humans. Most cases of infection tends to occur through use of hospital appliances such as catheters, I.V lines and breathing tubes in immunocompromised people.
• Steroid-dependant asthma: Steroid-dependant asthma refers to inflammation and constriction of the airways that can be managed only through regular use of oral steroids. Excessive use of steroids can lead to side effects so other therapies are often advised e.g. immunoglobulin therapy. The severity of symptoms is variable.
• Steroid-resistant asthma: Steroid-resistant asthma refers to inflammation and constriction of the airways that does not respond to treatment with steroids. However, higher than normal doses of steroids will alleviate symptoms in most patients but the higher doses carries an increased risk of side effects from steroid use. Other therapies such as immunoglobulin therapy is advised. The severity of symptoms is variable.
• Steroid-resistant asthma, type I: Steroid-resistant asthma is a type of asthma that doesn't respond to steroid treatment. Steroids work by attaching to a particular part of the T-cells which make up the immune system. In type I, the T-cells have sufficient attachment points for the steroids but they are ineffective. In type II, there are insufficient attachment points for the steroids. Steroid-resistant asthma (like other forms of asthma) involves rapid constriction and inflammation of the airways which makes breathing difficult.
• Steroid-resistant asthma, type II: Steroid-resistant asthma is a type of asthma that doesn't respond to steroid treatment. Steroids work by attaching to a particular part of the T-cells which make up the immune system. In type I, the T-cells have sufficient attachment points for the steroids but they are ineffective. In type II, there are insufficient attachment points for the steroids which make them less effective or completely ineffective. Steroid-resistant asthma (like other forms of asthma) involves rapid constriction and inflammation of the airways which makes breathing difficult.
• Steroid-sensitive asthma: Steroid-sensitive asthma refers to inflammation and constriction of the airways that responds well to treatment with steroids. The severity of symptoms is variable.
• Stevens Johnson syndrome: A rare but serious condition involving inflammation and blistering of the skin and mucous membranes. It is believed to be an allergic reaction that can occur in response to some drugs or infectious diseases.
• Stomach cancer: Stomach or gastric cancer can develop in any part of the stomach and may spread throughout the stomach and to other organs
• Stomach cancer, familial: Cancer of the stomach that tends to run in families.
• Storm syndrome: A rare progressive genetic disorder characterized by premature aging and heart disease which results in premature death.
• Streptococcal Group A invasive disease: Group A streptococci are bacteria which are commonly found in the throat or on the skin. Often it causes no symptoms but in some cases it can cause mild illnesses such as strep throat or more serious, life-threatening diseases such as toxic shock syndrome or flesh-eating disease. Transmission can occur through direct contact with infected skin sores or nose and throat discharges. Symptoms are determined by the location and extent of the bacterial infection.
• Streptococcal Group B invasive disease: Infection with bacteria called Group B Streptococcus which can cause severe symptoms or even death. The bacteria occur in the stomach and the urogenital tract of females and are normally harmless and cause no symptoms. However, it can cause a range of diseases in newborns, the elderly and people with poor immune systems.
• Streptococcal Infections: Various "strep" bacterial infections.
• Striatonigral degeneration infantile: A genetic neurological disorder caused by progressive damage to a part of the brain called the striatum.
• Striped Blister Beetle poisoning: The striped blister beetle is native to many parts of America and Canada. Animals that accidentally eat the beetles can become quite ill and they can also cause symptoms in humans if accidentally ingested. The beetles contain toxic substances called cantharidin and pederin which can cause symptoms through skin or eye exposure as well as through ingestion.
• Stroke symptoms: Brain-related symptoms of bleeding or blockage.
• Stuve-Wiedemann dysplasia: A rare syndrome characterized mainly by short stature, bowed long bones and permanent flexion of fingers.
• Stuve-Wiedemann syndrome: A rare syndrome characterized mainly by short stature, bowed long bones and permanent flexion of fingers.
• Subacute Sclerosing Panencephalitis: A progressive neurological disorder involving inflammation of the brain caused by a complication of the measles virus. It can occur up to 10 years after the initial measles virus and may be due to a defective immune response to the virus or a reactivation of the virus.
• Subacute sclerosing leukoencephalitis: A rare chronic form of brain inflammation that is associated with the measles virus. The patient usually appears to have a full recovery after the measles infection with symptoms developing usually between two and eight years after the infection. The condition tends to affect children and young adults mainly. The disease process involves the degeneration of the protective nerve sheaths (myelin) in the brain. Measles immunization is the most effective way of preventing the development of this complication of measles.
• Subaortic stenosis - short stature syndrome: A very rare syndrome characterized mainly by short stature and a narrowed portion of the aorta.
• Subdural hematoma: A condition which is characterized by a blood clot beneath the dura mater
• Succinic acidemia - lactic acidosis, congenital: A very rare disorder characterized by high levels of succinic acid in the blood and high blood acidity which starts at birth or soon after.
• Succinyl-CoA acetoacetate transferase deficiency: A very rare metabolic disorder involving an enzyme (Succinyl-CoA acetoacetate transferase) deficiency which prevents ketones being metabolized. Physical stress on the body (infection, exhaustion) can trigger an episode of ketosis, vomiting and rapid breathing.
• Sudden Arrhythmia Death Syndrome: A genetic heart disorder characterized by an abnormal heart rhythm which can result in sudden death in otherwise healthy people. It is caused by a genetic defect which affects the hearts electrical activity. Examples of disorders that can cause lethal heart rhythm abnormalities are Long QT syndrome, Brugada syndrome, certain drugs, idiopathic ventricular fibrillation and sodium channel disease.
• Sudden Infant Death Syndrome: The sudden death of an infant due to an unknown cause that occurs during sleep
• Sudden cardiac death: Sudden death that occurs due to a cardiac cause
• Sudden death: Death that occurs suddenly
• Sudden infant death syndrome: The sudden death of an infant due to an unknown cause that occurs during sleep
• Sudden unexpected death: The sudden and unexpected death of an individual
• Suicidal symptoms: Thoughts or actions toward suicide.
• Sulfa antibiotics allergy: Taking sulfa antibiotics can cause an allergic response in some people however this is considered rare. It involves the body's immune system overreacting to the drug. The type and severity of symptoms can vary considerable though skin symptoms are the most common allergic response to drugs.
• Sulfur tuft poisoning: Sulfur tuft is a type of small mushroom which can have yellow to orange to green caps. The mushroom has a very bitter taste and is poisonous - death can result if sufficient quantities are eaten.
• Sulphonamide -induced Immune Hemolytic Anemia: Sulphonamide-induced immune hemolytic anemia is a condition where use of a medication called Methyldopa triggers the body's immune system to destroy it's own red blood cells which results in anemia.
• Supraglottic laryngeal cancer: Cancer that arises in the tissue above the vocal cords.
• Surgical Wound Infection: Infection that occurs at the site of a surgery.
• Surma-induced lead poisoning: Surma is a black powder used as a cosmetic as well as a folk remedy by Middle East people to treat teething. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
• Sweetshrub poisoning: The sweetshrub is a large deciduous shrub which bears brownish-red flowers and seeds enclosed in a thick fiber casing. The plant may be found growing in the wild or in gardens as an ornamental plant. The crushed leaves have a strawberry odor. The seeds contain chemicals (calycanthin, alkaloids) which can cause symptoms if eaten in large quantities. The ingestion of large quantities by patients with underlying heart problems is more likely to cause symptoms.
• Swine flu: The Swine Flu is a respiratory viral disease which is usually found in pigs but can sometimes be transmitted to humans and cause epidemics or even pandemics. The viral strain involved is type A H1N1. The virus can be spread amongst humans from direct contact which can occur through coughing, sneezing or contamination of hands and surfaces. The severity of symptoms is highly variable, although with most people suffering only relatively mild symptoms. Patients are considered contagious for up to a week after the onset of symptoms but children may be contagious for longer periods of time.
• Symmetrical thalamic calcifications: A very rare disorder involving the calcification of a part of the brain called the thalamus which results in various abnormalities.
• Syncope: Loss or interruption of consciousness.
• Synovial cancer: Cancer (malignant) that develops in synovial tissue in joints. Synovial tissue can be found in the lining of cavities in joints, tendons and bursae.
• Syphilis: A sexually transmitted disease caused by a bacteria (Treponema pallidum). The condition is often asymptomatic in the early stages but one or more sores may be present in the early stages. Untreated syphilis usually results in remission of visible symptoms but further severe damage may occur to internal organs and other body tissues which can result in death.
• Systemic Capillary Leak Syndrome: A rare disease where episodes of leaking blood capillaries results in a rapid drop in blood pressure which can be life-threatening. Episodes usually last for a few days. The range and severity of symptoms experienced may range somewhat amongst patients.
• Systemic candidiasis: A candida infection that spreads throughout the body. If it invades major organs such as the brain and heart, death may result. It is rare in healthy individuals and tends to occur in immunocompromised individuals. The disorder is difficult to diagnose as it can invade almost any organ of the body and hence the symptoms are hugely variable.
• Systemic monochloroacetate poisoning: Monochloracetate acid is a dangerous chemical which can cause systemic poisoning even if only skin exposure occurs. Exposure to the chemical can be life-threatening with serious symptoms starting within hours of the exposure.
• T-cell acute lymphoblastic leukemia: Cancer of particular white blood cells called T-cells. Precursors to white blood cells are called blasts and are made by the bone marrow but in ALL the blasts are abnormal and do not develop into lymphocytes. Instead, the abnormal blasts or leukemic cells multiply rapidly and reduce the level of other types of blood cells such as red blood cells and platelets.
• TORCH Syndrome: Infection of a fetus by any of a group of infectious agents which have been transmitted from the mother through the placenta. The infections include toxoplasmosis, rubella, cytomegalovirus, herpes virus, hepatitis and syphilis. The severity and nature of symptoms is determined by the type of infection.
• Tako-Tsubo syndrome: Abnormal functioning of the left heart ventricle. It is a heart disease caused by extreme prolonged stress.
• Talon rodenticide poisoning: Talon is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Tapioca poisoning: Tapioca is a shrubby plant which bears inconspicuous flowers. The tubers contain chemicals (cyanogenic glycosides) which are turned into cyanide by the digestive process. Ingestion of the raw roots of this plant can result in death if sufficient quantities are eaten. The tubers are edible if they are boiled first. Toxicity varies within the species depending on growing conditions and other factors.
• Tarpon poisoning (clupeotoxin): Some tarpon contain toxins (Clupeotoxin) which can be poisonous to humans if eaten. Heat does not destroy the toxin and there is still uncertainty as to the origin of the toxin. The toxin appears to be present in higher concentrations in summer and is believed to be possible linked to the consumption of toxic food in its food web. The size and age of the tarpon does not appear to be related to the toxicity. The tarpon are found in coastal waters off Africa and the Caribbean, Indian and Pacific Oceans.
• Temtamy syndrome: A rare disorder characterized by a brain abnormality, unusual facial appearance and eye coloboma.
• Tetanus: A disease caused by chemicals which are produced by a bacterium (clostridium tetani) and are toxic to the nerves. The infection usually occurs when the bacteria enter the body through a deep wound - these bacteria are anaerobic and hence don't need oxygen to survive.
• Tetraamelia - multiple malformations: A very rare syndrome characterized mainly by a lack of arm and leg bones (hands and feet are still present) as well as other malformations.
• Tetraamelia with pulmonary hypoplasia: A very rare syndrome characterized mainly by the absence of arms and legs and abnormal lung development.
• Tetraploidy: A very rare chromosomal disorder which results in various abnormalities. Infants are usually stillborn or die within months of birth.
• Thakker-Donnai syndrome: A very rare, severe genetic syndrome characterized by abnormal internal organs and facial anomalies.
• Thalamic degeneration symmetrical infantile: A very rare brain disorder characterized by abnormal brain development, seizures, respiratory distress and movement disorders.
• Thanatophoric dysplasia, Glasgow variant: A lethal form of dwarfism.
• Thin ribs - tubular bones - dysmorphism: A very rare syndrome characterized mainly by thin ribs, narrow-shafted long bones and a large head.
• Thomas-Jewett-Raines syndrome: A very rare syndrome characterized mainly by small eyes, small ears and a lack of fetal movement.
• Thompson-Baraitser syndrome: A very rare syndrome characterized mainly by liver fibrosis, kidney cysts and mental retardation.
• Thoraco abdominal enteric duplication: A very rare syndrome characterized by chest and abdominal abnormalities as well as intestinal duplication.
• Thoracopelvic dysostosis: A rare syndrome characterized mainly by abnormalities involving the chest, larynx and pelvis. The small chest cavity affects breathing and can affect survival, especially during infancy.
• Thromboembolism: Lodgement of a blood clot causing blockage
• Thrombomodulin anomalies, familial: A defect in a protein involved with anticoagulation which results in an increased risk of developing blood clots which can result in death.
• Thymic epithelial tumor: A tumor that develops in the outer layers (epithelial) layers of the thymus. The tumor may be malignant or benign. The thymus produces white blood cells.
• Thymic-Renal-Anal-Lung dysplasia: A rare syndrome characterized by abnormalities involving the lungs, anus, kidneys and thymus.
• Thyroid cancer, Hurthle cell: A rare form of cancer that originates in the thyroid gland. This cancer is characterized by the abnormal presence of Hurthle cells which may signify benign or malignant thyroid cancer. The cancer usually responds well to treatment if detected in the earlier stages.
• Thyroid cancer, anaplastic: A thyroid gland cancer that is quite aggressive and metastasizes to other parts of the body.
• Thyroid cancer, follicular: A usually slow-growing cancer of the thyroid gland which is rarely fatal. The cancer develops from cells in the thyroid that produce iodine-containing hormones. This type of cancer usually responds well to treatment.
• Thyroid cancer, medullary: Cancer of the thyroid gland. The cancer develops from the parafollicular cells or in the thyroid gland which produced calcitonin. This type of cancer does not respond to treatment as well as papillary or follicular thyroid cancer. This form of thyroid cancer may be inherited.
• Thyroid cancer, papillary: A usually slow-growing cancer of the thyroid gland which is rarely fatal. The cancer develops from cells in the thyroid that produce iodine-containing hormones. This type of cancer usually responds well to treatment.
• Timothy syndrome: A rare syndrome characterized by webbed fingers and a heart defect. Most affected individuals die during early childhood or infancy.
• Tobacco smoke associated asthma: Tobacco smoke associated asthma refers to inflammation and constriction of the airways that is caused by exposure to tobacco smoke. The severity of symptoms is variable.
• Togaviridae disease: Infection with any of a number of togaviridae viruses which can caused conditions such as Equine encephalitis, Ross River virus and Rubella virus. Symptoms are determined by the type of virus involved. Togaviridae are arboviruses and are transmitted by arthropods.
• Tollner-Horst-Manzke syndrome: A very rare syndrome characterized by extra fingers, cleft lip, cleft palate and abdominal organ anomalies.
• Tolterodine toxicity: The toxic reaction of the body to the substance, possibly via allergic reaction or overdose.
• Toxic Shock Syndrome: Severe immune reaction causing shock
• Toxic epidermal necrolysis: A skin condition causing widespread blisters to erupt over greater than 30% of the body.
• Toxic mushrooms - Anticholinergic: Some mushrooms contain a toxic chemical called ibotenic acid which causes anticholinergic symptoms. Ibotenic acid is converted to muscimol during digestion. The two toxins have opposing actions which results in initial excitation symptoms followed by a prolonged coma-like sleep. Mushroom species from this group include certain species of Amanita sp. - cothurnata, crenulata, frostiana, gemmata, muscaria and pantherina. Eating two to four mushrooms can result in impaired senses and eating more than twenty usually results in death.
• Toxic mushrooms - Monomethylhydrazine: Some mushrooms contain a toxic chemical called gyromitrin which is converted to monomethylhydrazine after digestion. Mushroom species from this group include certain species of Gyromitra, Helvella, Sarcosphaera and Peziza. Poisoning may occur from inhaling fumes from cooking mushrooms. The amount of toxin varies amongst and within species but some are toxic enough to cause death. Urgent medical attention should be sought if mushroom poisoning is suspected.
• Toxic mushrooms - Renal toxic (orelline): Some mushrooms (Amanita smithiana) contain chemicals (allenic norleucine, chlorocrotyglycine) which can cause kidney damage.
• Toxic mushrooms - cyclopeptides: Some mushrooms contain a toxic chemical called cyclopeptide which can cause primarily gastrointestinal symptoms if ingested. Most cases of mushroom poisoning in North America involve cyclopeptide-containing mushrooms. Mushroom species from this group include certain species of Amanita (bisporigera, ocreata, phalloides, suballiacea, tenufolia, verna, virosa), Galerina and Lepiota. One Amanita mushroom cap may result in death in an adult. Poisoning occurs in three phases: gastrointestinal symptoms (within 24 hours of ingestion); remission (up to 72 hours after ingestion); and liver and kidney symptoms (3 to 6 days after ingestion). Poisoning symptoms are more severe in children due to their smaller body size.
• Tracheal agenesis without tracheoesophageal fistula: A rare condition characterized by an underdeveloped or absent trachea. There is no associated opening connecting the trachea to the esophagus. The condition is incompatible with life. There are three subtypes of the disorder depending on the specific tracheal defect.
• Tracheoesophageal fistula - hypospadias: A rare syndrome characterized by an abnormal opening between the trachea and esophagus and abnormal positioning of urethral opening in males.
• Tranquilizer addiction: An uncontrollable desire to use tranquilizers on a regular basis. Tranquilizers are often prescribed for the treatment of anxiety and sleeping problems but chronic use can lead to dependence on the drug. Frequent use leads to an increased tolerance to the drug so higher and higher doses are required to achieve the desired euphoric feeling.
• Transient Neonatal Myasthenia Gravis: Myasthenia gravis is a chronic neuromuscular disease resulting from autoimmune dysfunction. In transient neonatal myasthenia gravis muscle weakness occurs only for a period of time after birth. The condition occurs in infants of mothers with myasthenia gravis. Symptoms will persist in the infant until the antibodies from the mother which cause the muscle weakness disappear. The severity of the condition in the mother does not seem to reflect the severity of symptoms in offspring.
• Transplacental infections: An infection that passes from the mother to the fetus via the placenta. A large variety of infections can occur like this and the type and severity of symptoms can vary greatly depending on the type of infection and the stage of fetal development at which infection occurs. Examples of transplacental infections include cytomegalovirus, herpes virus, hepatitis, syphilis, toxoplasmosis and rubella.
• Transposition of great arteries: A congenital malformation where the aorta and pulmonary artery are transposed which causes oxygenated blood from the lungs to be sent back to the lungs and de-oxygenated blood to be sent to body tissues. Often there is some other defect such as an opening in the heart chambers which allows mixing of the blood and hence survival is possible for a short while at least.
• Traumatic Brain Injury: Brain injury from trauma or accident.
• Treponema infection: A rare infectious diseases which is transmitted through sexual contact and caused by Treponema pallidum (a spirochete bacterium). Untreated cases can result in severe complications and even death.
• Tricho-hepato-enteric syndrome: A very rare syndrome characterized mainly by hair and liver abnormalities as well as severe diarrhea that usually starts in early infancy and can lead to death.
• Trichosporin infection: A very rare infectious disease caused by the Trichosporon species. This type of infection tends to be opportunistic and hence only affects patients who are immunocompromised - patients with blood cancers appear to be the most prone. The infection may be localized or spread throughout the body (disseminated) which is usually fatal. Symptoms and severity may vary considerably depending on the location and extent of the infection.
• Triggerfish poisoning (Palytoxin): Palytoxin is a marine toxin found in some triggerfish from the Philippines region. The toxin is extremely potent and death is common in patients who ingest contaminated triggerfish.
• Triose phosphate-isomerase deficiency: A very rare inherited condition involving a deficiency of triose phosphate-isomerase.
• Triosephosphate isomerase 1: A rare inherited blood disorder involving a deficiency of red cell triosephosphate isomerase which is involved in the glycolysis (glucose metabolism) process to produce energy. The disorder is characterized by anemia, recurring infection and often progressive neurological degeneration. The severity of the disorder is variable with some patients having central nervous system involvement while others don't.
• Triploid syndrome: A complete extra set of chromosomes.
• Trisomy 10 mosaicism: A very rare chromosomal disorder where there is an extra copy of chromosome 10 in some of the body's cells. Some cases with this chromosomal abnormality have no clinical symptoms. The presence of abnormalities in some cases is dependent on which body cells contain the chromosomal defect.
• Trisomy 12 mosaicism: A very rare chromosomal disorder where there is an extra copy of chromosome 12 in some of the body's cells. Some cases with this chromosomal abnormality have no clinical symptoms. The presence of abnormalities in some cases is dependent on which body cells contain the chromosomal defect.
• Trisomy 13 mosaicism: A very rare chromosomal disorder where there is an extra copy of chromosome 13 in some of the body's cells. Some cases with this chromosomal abnormality have no clinical symptoms. The presence of abnormalities in some cases is dependent on which body cells contain the chromosomal defect. There appears to be a direct correlation between the number of cells in the body containing the chromosomal defect and severity of symptoms and survival.
• Trisomy 18 Syndrome: A rare genetic chromosomal syndrome where the child has an extra third copy of chromosome 18. Most fetuses are aborted before term, but a live birth with this condition occurs with a frequency around 1-in-3000. Edwards syndrome is more severe than the more common Down syndrome. Edwards syndrome causes mental retardation and numerous physical defects that often cause an early infant death. The condition has variable severity depending on how many of the body's cells have the extra chromosome and how much of the extra chromosome is duplicated. In severe forms all cells have an extra copy of the complete chromosome 18 whereas milder forms may have only some cells having the extra chromosome. Other mild forms may have an extra copy of only part of chromosome 18 in some or all of the body cells.
• Trisomy 18 mosaicism: A rare genetic chromosomal syndrome where the child has an extra third copy of chromosome 18 in only some of the body's cells. It is a less severe form of Edwards syndrome - the most severe form involves and extra copy of chromosome 18 in all of the body's cells. The severity of the condition is highly variable depending on how many of the body's cells are involved.
• Trisomy 20 mosaicism: A very rare chromosomal disorder where there is an extra copy of chromosome 20 in some of the body's cells. Some cases with this chromosomal abnormality have no clinical symptoms. The presence of abnormalities in some cases is dependent on which body cells contain the chromosomal defect.
• Trisomy 3 mosaicism: A very rare chromosomal disorder where there is an extra copy of chromosome 3 in some of the body's cells. Some cases with this chromosomal abnormality have no clinical symptoms. The presence of abnormalities in some cases is dependent on which body cells contain the chromosomal defect.
• Trisomy 4 mosaicism: A very rare chromosomal disorder where there is an extra copy of chromosome 4 in some of the body's cells. Some cases with this chromosomal abnormality have no clinical symptoms. The presence of abnormalities in some cases is dependent on which body cells contain the chromosomal defect.
• Trisomy 8 mosaicism: A very rare chromosomal disorder where there is an extra copy of chromosome 8 in some of the body's cells. Some cases with this chromosomal abnormality have no clinical symptoms. The presence of abnormalities in some cases is dependent on which body cells contain the chromosomal defect.
• Tropical Reef Crab poisoning: The tropical reef crab is commonly found and eaten in the Indo-Pacific region. These crabs can contain toxic chemicals which can cause severe poisoning in humans if eaten. The best way to avoid poisoning is to not eat these crabs at all.
• Trumpet flower poisoning: The trumpet flower is a flowering vine-like plant that bears fairly large, colorful, trumpet-shaped flowers. It is often grown in gardens as an ornamental plant. The leaves and flowers of the plant contain chemicals (solanine, solanidine) which are highly toxic. Ingestion of sufficient flowers and leaves can result in death.
• Trypanosomiasis, east-African: A rare infectious disease caused by a parasite called Trypanosoma brucei rhodesiense and is transmitted through the bite of an infected Tsetse fly. The infection causes an acute illness with symptoms occurring from days to weeks after infection. Death relatively common, especially in untreated cases.
• Tubatoxin poisoning: Tubatoxin is a naturally occurring chemical found in certain plants (Derris and Lonchocarpus sp.). It gives the plant insecticidal and pesticidal properties and is hence utilized commercially as an insecticide. Ingestion and other exposures to the chemical can cause various symptoms. Inhalation tends to cause more severe symptoms than ingestion. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Tuberculosis: Bacterial infection causing nodules forming, most commonly in the lung.
• Tuberculous pericarditis: Inflammation and swelling of the pericardium (fibrous sac surrounding the heart) that occurs as a complication of tuberculosis. The condition may be misdiagnosed as a heart attack and vice versa.
• Tumor lysis syndrome: Metabolic abnormalities that can occur when chemotherapy drugs rapidly destroy tumor cells.
• Tung oil tree poisoning: Tung oil tree is a deciduous tree with dark green leaves and pink to white flowers with a darker centre. The plant originated in China and is often used in gardens as an ornamental plant. The plant (especially the seeds) contain chemicals (glycoside and others) which can cause serious symptoms and even death if sufficient quantities are eaten.
• Type 1 Tracheal agenesis without tracheoesophageal fistula: A rare condition characterized by an underdeveloped or absent trachea. Type 1 is distinguished by a fibrous cord replacing the trachea making breathing impossible. There is no associated opening connecting the trachea to the esophagus. The condition is incompatible with life.
• Type 10 17b-hydroxysteroid dehydrogenase deficiency: A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Symptoms tend to be more severe in males who suffer progressive neurodegeneration whereas females tend to suffer mainly from developmental delay.
• Type 2 Tracheal agenesis without tracheoesophageal fistula: A rare condition characterized by an underdeveloped or absent trachea. Type 2 is distinguished by a complete absence of the trachea but the main bronchi join at the carina in the middle. There is no associated opening connecting the trachea to the esophagus. The condition is incompatible with life as breathing is impossible.
• Type 3 Tracheal agenesis without tracheoesophageal fistula: A rare condition characterized by an underdeveloped or absent trachea. Type 3 is distinguished by a complete absence of the trachea and the main bronchi don't join at the carina in the middle but run separately to the esohagus. There is no associated opening connecting the trachea to the esophagus. The condition is incompatible with life as breathing is impossible.
• Type A Influenza: Type A influenza is a subtype of the influenza virus that can cause cause serious illness and result in pandemics. Influenza is viral respiratory infection. The virus is very contagious and can cause severe illness especially in patients who are very young or old or have some other medical condition as well. The severity of symptoms can vary but usually involves respiratory and constitutional (e.g. headache, aching muscles) symptoms. The influenza virus can mutate and produce different strains though the symptoms are the same. This frequent mutation means that people need regular vaccinations to ensure they are protected against new strains as they arise.
• Type A influenza subtype H1: The H1 subtype of influenza is a strain of the type A influenza virus that can cause cause serious illness and result in pandemics. Influenza is viral respiratory infection. The virus is very contagious and can cause severe illness especially in patients who are very young or old or have some other medical condition as well. The severity of symptoms can vary but usually involves respiratory and constitutional (e.g. headache, aching muscles) symptoms. The influenza virus can mutate and produce different strains though the symptoms are the same. This frequent mutation means that people need regular vaccinations to ensure they are protected against new strains as they arise.
• Type A influenza subtype H10N7: Influenza is viral respiratory infection. The virus is very contagious and can cause severe illness especially in patients who are very young or old or have some other medical condition as well. The severity of symptoms can vary but usually involves respiratory and constitutional (e.g. headache, aching muscles) symptoms. The influenza virus can mutate and produce different strains though the symptoms are the same. This frequent mutation means that people need regular vaccinations to ensure they are protected against new strains as they arise. Influenza A H10N7 is a subtype of influenza which rarely causes infection in human - only two cases of infectin have been reported.
• Type A influenza subtype H1N1: The H1N1 subtype of influenza is a strain of the type A influenza virus that can cause illness in humans. Influenza is viral respiratory infection. The virus is contagious and can cause severe illness especially in patients who are very young or old or have some other medical condition as well. The severity of symptoms can vary but usually involves respiratory and constitutional (e.g. headache, aching muscles) symptoms. The H1N1 subtype caused a pandemic called the Spanish Flu in 1918 and resulted in millions of deaths.
• Type A influenza subtype H1N2: The H1N2 subtype of influenza is a strain of the type A influenza virus that can cause cause illness in humans. Influenza is viral respiratory infection. The virus is contagious and can cause severe illness especially in patients who are very young or old or have some other medical condition as well. The severity of symptoms can vary but usually involves respiratory and constitutional (e.g. headache, aching muscles) symptoms. The influenza virus can mutate and produce different strains though the symptoms are the same. This frequent mutation means that people need regular vaccinations to ensure they are protected against new strains as they arise.
• Type A influenza subtype H2N2: The H2N2 subtype of influenza is a strain of the type A influenza virus that can cause cause illness in humans. Influenza is viral respiratory infection. The virus is very contagious and can cause severe illness especially in patients who are very young or old or have some other medical condition as well. The severity of symptoms can vary but usually involves respiratory and constitutional (e.g. headache, aching muscles) symptoms. The influenza virus can mutate and produce different strains though the symptoms are the same. This frequent mutation means that people need regular vaccinations to ensure they are protected against new strains as they arise.
• Type A influenza subtype H3N2: The H3N2 subtype of influenza is a strain of the type A influenza virus that can cause cause illness in humans. Subtype H3N2 has caused a number of pandemics (e.g. Hong Kong Flu) and tends to occur in a seasonal pattern in many parts of the world. Influenza is viral respiratory infection. The virus is very contagious and can cause severe illness especially in patients who are very young or old or have some other medical condition as well. The severity of symptoms can vary but usually involves respiratory and constitutional (e.g. headache, aching muscles) symptoms. The influenza virus can mutate and produce different strains though the symptoms are the same. This frequent mutation means that people need regular vaccinations to ensure they are protected against new strains as they arise.
• Type A influenza subtype H5: Influenza is viral respiratory infection. The virus is very contagious and can cause severe illness especially in patients who are very young or old or have some other medical condition as well. The severity of symptoms can vary but usually involves respiratory and constitutional (e.g. headache, aching muscles) symptoms. The influenza virus can mutate and produce different strains though the symptoms are the same. This frequent mutation means that people need regular vaccinations to ensure they are protected against new strains as they arise. Influenza A H5 is a subtype of influenza which can be further divided into subtypes e.g. H5N1.
• Type A influenza subtype H5N1: Influenza is viral respiratory infection. The virus is very contagious and can cause severe illness especially in patients who are very young or old or have some other medical condition as well. The severity of symptoms can vary but usually involves respiratory and constitutional (e.g. headache, aching muscles) symptoms. The influenza virus can mutate and produce different strains though the symptoms are the same. This frequent mutation means that people need regular vaccinations to ensure they are protected against new strains as they arise. Influenza A H5N1 is a subtype of influenza that mainly infects birds but can be transmitted to humans. Infections were reported in Hong Kong in 1997 and in various parts of the world in 2003 - 2007.
• Type A influenza subtype H7: Influenza is viral respiratory infection. The virus is very contagious and can cause severe illness especially in patients who are very young or old or have some other medical condition as well. The severity of symptoms can vary but usually involves respiratory and constitutional (e.g. headache, aching muscles) symptoms. The influenza virus can mutate and produce different strains though the symptoms are the same. This frequent mutation means that people need regular vaccinations to ensure they are protected against new strains as they arise. Influenza A H7 is a subtype of influenza which usually infects animals but can be transmitted to humans.
• Type A influenza subtype H7N2: Influenza is viral respiratory infection. The virus is very contagious and can cause severe illness especially in patients who are very young or old or have some other medical condition as well. The severity of symptoms can vary but usually involves respiratory and constitutional (e.g. headache, aching muscles) symptoms. The influenza virus can mutate and produce different strains though the symptoms are the same. This frequent mutation means that people need regular vaccinations to ensure they are protected against new strains as they arise. Influenza A H7N2 is a subtype of influenza which has rarely infected humans. Infections were reported in New York in 2003 and in the UK in 2007.
• Type A influenza subtype H7N3: Influenza is viral respiratory infection. The virus is very contagious and can cause severe illness especially in patients who are very young or old or have some other medical condition as well. The severity of symptoms can vary but usually involves respiratory and constitutional (e.g. headache, aching muscles) symptoms. The influenza virus can mutate and produce different strains though the symptoms are the same. This frequent mutation means that people need regular vaccinations to ensure they are protected against new strains as they arise. Influenza A H7N3 is a subtype of influenza which rarely infects humans. Infections were reported were reported in Canada in 2004.
• Type A influenza subtype H7N7: Influenza is viral respiratory infection. The virus is very contagious and can cause severe illness especially in patients who are very young or old or have some other medical condition as well. The severity of symptoms can vary but usually involves respiratory and constitutional (e.g. headache, aching muscles) symptoms. The influenza virus can mutate and produce different strains though the symptoms are the same. This frequent mutation means that people need regular vaccinations to ensure they are protected against new strains as they arise. Influenza A H7N7 is a subtype of influenza which rarely infects humans. Infections were reported in the UK in 1996 and in the Netherlands in 2003.
• Type A influenza subtype H9: Influenza is viral respiratory infection. The virus is very contagious and can cause severe illness especially in patients who are very young or old or have some other medical condition as well. The severity of symptoms can vary but usually involves respiratory and constitutional (e.g. headache, aching muscles) symptoms. The influenza virus can mutate and produce different strains though the symptoms are the same. This frequent mutation means that people need regular vaccinations to ensure they are protected against new strains as they arise. Influenza A H9 is a subtype of influenza which rarely causes infection in humans and tends to only cause mild illness.
• Type A influenza subtype H9N2: Influenza is viral respiratory infection. The virus is very contagious and can cause severe illness especially in patients who are very young or old or have some other medical condition as well. The severity of symptoms can vary but usually involves respiratory and constitutional (e.g. headache, aching muscles) symptoms. The influenza virus can mutate and produce different strains though the symptoms are the same. This frequent mutation means that people need regular vaccinations to ensure they are protected against new strains as they arise. Influenza A H9N2 is a subtype of influenza which rarely causes infection in humans. A small number of cases occurred in China and Hong Kong in 1999 and 2003 and 2007.
• Type B Influenza: Type B influenza is a subtype of the influenza virus that tends to occur sporadically - can cause epidemics but not pandemics. Influenza is viral respiratory infection. The virus is very contagious and can cause severe illness especially in patients who are very young or old or have some other medical condition as well. The severity of symptoms can vary but usually involves respiratory and constitutional (e.g. headache, aching muscles) symptoms. The influenza virus can mutate and produce different strains though the symptoms are the same. This frequent mutation means that people need regular vaccinations to ensure they are protected against new strains as they arise.
• Type C Influenza: Type C influenza is a subtype of the influenza virus that only rarely infects people and tends to only cause mild illness. It is not known to cause epidemics or pandemics. Influenza is viral respiratory infection.
• Type I Hyperlipoproteinemia: Type I Hyperlipoproteinemia is a rare inherited condition characterized by high levels of chylomicrons (a type of lipoprotein) in the blood. This condition is the result of low levels of lipoprotein lipase which is responsible for lowering lipoprotein levels. Cholesterol levels are usually normal and the risk of heart disease is low.
• Type I Hypersensitivity: Type I hypersensitivity is an exaggerated response by the body's immune system to an allergen which results in some sort of adverse effect on the body. Allergens usually in the form of proteins such as pollen, foods, house dust mite and cat hair. This form of hypersensitivity results in an immediate response by the immune system following exposure.
• Type II Hyperlipoproteinemia: Type II Hyperlipoproteinemia is a condition characterized by high levels of beta-lipoproteins in the blood. The high cholesterol results from abnormally high levels of low density lipoproteins in the blood due to a deficiency of LDL receptors. There are two subtypes of this condition: type IIa and type IIb. Lipoproteins are responsible for transporting cholesterol in the bloodstream and high levels of them in the bloodstream means that there are high levels of cholesterol in the bloodstream.
• Type III Hyperlipoproteinemia: Type III hyperlipoproteinemia is a rare genetic condition characterized by increased blood levels of intermediate density lipoproteins (IDL) which in turn causes high cholesterol levels. The high IDL levels are caused by an abnormality in apolipoprotein E. Apolipoprotein E is a protein found on IDLs which allows the IDLs to bind to liver cells. Without this binding process, the level of IDLs in the blood increase. Lipoproteins are responsible for transporting cholesterol in the bloodstream and high levels of them in the bloodstream means that there are high levels of cholesterol in the bloodstream.
• Type IIa Hyperlipoproteinemia: Familial Hyperlipoproteinemia is a rare genetic condition characterized by high levels of low density lipoproteins in the blood. A deficiency of LDL receptors leads to an increased level of low density lipoproteins (LDLs) which in turn causes high cholesterol levels. Lipoproteins are responsible for transporting cholesterol in the bloodstream and high levels of them in the bloodstream means that there are high levels of cholesterol in the bloodstream.
• Type IIb Hyperlipoproteinemia: Type IIb Hyperlipoproteinemia is a condition characterized by increased blood levels of low density lipoproteins (LDL) and apoprotein B (ApoB). This in turn causes high cholesterol levels. Lipoproteins are responsible for transporting cholesterol in the bloodstream and high levels of them in the bloodstream means that there are high levels of cholesterol in the bloodstream.
• Type IV Hyperlipoproteinemia: Type IV Hyperlipoproteinemia is an inherited condition characterized by high levels of very low density lipoproteins (VLDL) in the blood which in turn causes high cholesterol levels. Lipoproteins are responsible for transporting cholesterol in the bloodstream and high levels of them in the bloodstream means that there are high levels of cholesterol in the bloodstream. The high VLDL levels are a result of increased production and reduced elimination of the VLDLs. Environmental factors are the driving force behind this condition.
• Type Ia Hyperlipoproteinemia: Type Ia Hyperlipoproteinemia is a rare inherited condition characterized by high levels of chylomicrons (a type of lipoprotein) in the blood. This condition is the result of low levels of lipoprotein lipase which is responsible for lowering lipoprotein levels. Cholesterol levels are usually normal and the risk of heart disease is low.
• Type Ib Hyperlipoproteinemia: Type Ib Hyperlipoproteinemia is a rare inherited condition characterized by high levels of chylomicrons (a type of lipoprotein) in the blood. This condition is the result of low levels of apolipoprotein C-II which is responsible for lowering lipoprotein levels. Cholesterol levels are usually normal and the risk of heart disease is low.
• Type Ic Hyperlipoproteinemia: Type Ic Hyperlipoproteinemia is a rare inherited condition characterized by high levels of chylomicrons (a type of lipoprotein) in the blood. This condition is the result of inhibited lipoprotein lipase activity. Lipoprotein lipase is responsible for lowering lipoprotein levels. Cholesterol levels are usually normal and the risk of heart disease is low.
• Type V Hyperlipoproteinemia: Type V Hyperlipoproteinemia is a rare condition characterized by increased synthesis of very low density lipoproteins (VLDL) and reduced levels of lipoprotein lipase (an enzyme). Lipoproteins are responsible for transporting cholesterol in the bloodstream and high levels of them in the bloodstream means that there are high levels of cholesterol in the bloodstream.
• Typhoid fever: Fever from bacterial food poisoning.
• Uhl anomaly: A rare congenital heart malformation where the myocardial layer (muscle wall of the heart) of the right ventricle is completely or partially absent.
• Unverricht-Lundborg disease: A rare inherited type of progressive myoclonus epilepsy which tends to cause symptoms during childhood. The involuntary muscle movements tend to occur more frequently and become more severe with increasing age. Symptoms may occur following various stimuli such as light, stress or exercise.
• Unverricht-Lundborg syndrome: A rare inherited type of progressive myoclonus epilepsy which tends to cause symptoms during childhood. The involuntary muscle movements tend to occur more frequently and become more severe with increasing age. Symptoms may occur following various stimuli such as light, stress or exercise.
• Urachal cancer: A very rare cancer that occurs in the top of the urinary bladder. The urachus is a tube which joins the belly button to the top of the bladder. After birth, this tube gradually disappears and the amount remaining varies from person to person.
• Uremia: Build up of toxins usually excreted by the kidneys, associated with real failure in a woman who is pregnant.
• Uremic pericarditis: Inflammation and swelling of the pericardium (fibrous sac surrounding the heart) that occurs as a complication in people with uremia. Uremia is a buildup of urea and other waste material in the blood due to kidney failure. Uremic pericarditis condition may be misdiagnosed as a heart attack and vice versa.
• Urethral cancer: A rare cancer that develops in the urethra which carries urine from the bladder to be excreted.
• Urethral obstruction sequence: A condition which is characterised by the early obstruction of the urethra.
• Urinary tract neoplasm: A tumor that develops anywhere along the urinary tract. The urinary tract includes the kidneys, urethra and ureters. The tumor may be malignant or benign.
• Urophathy distal obstructive polydactyly: A rare syndrome characterized by extra digits and an obstructive urinary system disorder.
• Uterine Hemorrhage: Bleeding from the uterus. Often occurs as a complication of childbirth or fibroids. The severity of the condition depends on the amount and rate of blood loss.
• Uterine sarcoma: A rare type of cancer that occurs in the uterus or associated tissues. A sarcoma is a cancer that involves soft tissue and connective tissue such as bone, cartilage, fat, muscle and blood vessels.
• VACTERL with hydrocephalus, X-linked: A rare X-linked syndrome characterized by the VACTERL abnormalities (vertebral anomalies, anal atresia, congenital cardiac disease, tracheoesophageal fistula, renal anomalies, radial dysplasia, limb defects) as well as a buildup of fluid inside the skull (hydrocephalus).
• Vaccinia: A cowpox virus that was initially used for human smallpox vaccines.
• Vaccinia gangrenosa: Vaccinia gangrenosa is a serious complication of smallpox vaccination. The condition involves progressive death of tissue (necrosis) at the site of the vaccination. The condition is relatively rare but can result in death so prompt diagnosis and treatment is essential. People with AIDS, immunodeficiencies, cancer, receiving immunosuppressive therapies or have some other form of immune system defect are particularly susceptible to this complication.
• Vaccinia necrosum: Vaccinia necrosum is a serious complication of smallpox vaccination. The condition involves progressive death of tissue (necrosis) at the site of the vaccination. The condition is relatively rare but can result in death so prompt diagnosis and treatment is essential. People with AIDS, immunodeficiencies, cancer, receiving immunosuppressive therapies or have some other form of immune system defect are particularly susceptible to this complication.
• Vacuolar Cardiomyopathy and Myopathy, X-linked: A rare inherited disorder characterized by severe heart problems, varying degrees of muscle weakness and often mental retardation. Other symptoms such as mental retardation may also occur. The genetic anomaly manifests as a deficiency of a protein called LAMP-2 (Lysosomal-Associated Membrane Protein 2) which affects lysosomes.
• Vagal Paraganglioma: A rare, usually benign tumor found in the neck. The tumor develops from glomus cells which are located along blood vessels involved in automatic body activities such as regulation of blood pressure and blood flow.
• Valproic Acid - Teratogenic Agent: There is evidence to indicate that exposure to Valproic Acid during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
• Van Bogaert disease: A rare inherited condition where cholesterol is deposited in the brain and other parts of the body. The disease is classified as a lipid storage disorder due to the abnormal deposition of cholesterol and cholestanol in various parts of the body - especially the brain, lungs and Achilles tendon. The condition is possibly highly underdiagnosed.
• Van Bogaert's disease: A rare inherited condition where cholesterol is deposited in the brain and other parts of the body. The disease is classified as a lipid storage disorder due to the abnormal deposition of cholesterol and cholestanol in various parts of the body - especially the brain, lungs and Achilles tendon. The condition is possibly highly underdiagnosed.
• Van Bogaert-Scherer-Epstein Disease: A rare inherited condition where cholesterol is deposited in the brain and other parts of the body. The disease is classified as a lipid storage disorder due to the abnormal deposition of cholesterol and cholestanol in various parts of the body - especially the brain, lungs and Achilles tendon. The condition is possibly highly underdiagnosed.
• Vanishing white matter leukodystrophy: Degeneration of the brain white matter. The condition tends to progress relatively slowly but a sudden deterioration of symptoms can occur after a head trauma or an illness involving fever. Some degree of recovery can occur after the sudden deterioration but other cases can result in coma and death. Survival is possible into the third decade.
• Variceal Bleeding: Bleeding that occurs in dilated blood vessels that usually develop in the esophagus or stomach. The dilated blood vessels are asymptomatic unless they burst which can then become a life-threatening condition. Bleeding varices are most often caused by liver cirrhosis which increases the blood pressure in the veins that carry blood from the digestive organs to the liver.
• Vasculitis hypersensitivity: A condition which is characterised by a reaction that results in the inflammation of the blood vessels
• Venerupin shellfish poisoning: The venerupin shellfish can be eaten by humans. The shellfish can become toxic if they consume toxic algae. The shellfish is most commonly found and eaten in Japan but has been introduced into parts of the US. Interestingly, all cases of poisoning have occurred in very localized areas of Japan where they are harvested from lakes. This type of poisoning tends to have a high death rate - up to a third of patients die.
• Venezuelan equine encephalitis: A mosquito-borne virus that usually affects horses and related animals but may also infect humans. Young, weak and old people may become very sick and in some cases death can occur. It occurs in Central and South America. The incubation period is 2-5 days. The period of illness is usually 3-8 days but relapses are possible.
• Ventricular tachycardia, catecholaminergic polymorphic, 1: A very rare inherited heart disorder involving an abnormal heart rhythm in an apparently otherwise normal heart. Sudden death can occur readily. Symptoms such as fainting and seizures can be triggered by strenuous physical activity or sudden excitement. Type 1 is caused by a defect in the RYR2 gene on chromosome 1q42.1-q43.
• Ventricular tachycardia, catecholaminergic polymorphic, 2: A very rare, recessively inherited heart disorder involving an abnormal heart rhythm in an apparently otherwise normal heart. Sudden death can occur readily. Symptoms such as fainting and seizures can be triggered by strenuous physical activity or sudden excitement. Type 2 is caused by a defect in the CASQ2 gene on chromosome 1p13.3-p11.
• Very Long Chain Acyl CoA Dehydrogenase Deficiency - Early onset: Very Long Chain Acyl CoA Dehydrogenase Deficiency is a rare inherited genetic condition where the body is unable to convert certain fats to energy i.e. there is not enough of a certain enzyme which is needed to metabolize a type of fat called long-chain fatty acids. The build-up of these fatty acids in the body causes damage. There are three subtypes of the disorder each with varying severity: severe early-onset form, an intermediate form and an adult-onset form. The early-onset form is the most severe and can readily lead to death if undiagnosed.
• Very Long Chain Acyl CoA Dehydrogenase Deficiency - adult-onset: Very Long Chain Acyl CoA Dehydrogenase Deficiency is a rare inherited genetic condition where the body is unable to convert certain fats to energy i.e. there is not enough of a certain enzyme which is needed to metabolize a type of fat called long-chain fatty acids. The build-up of these fatty acids in the body causes damage. There are three subtypes of the disorder each with varying severity: severe early-onset form, an intermediate form and an adult-onset form. The adult-onset form is relatively mild and tends to be characterized mainly by muscle problems.
• Very Long Chain Acyl CoA Dehydrogenase Deficiency - intermediate: Very Long Chain Acyl CoA Dehydrogenase Deficiency is a rare inherited genetic condition where the body is unable to convert certain fats to energy i.e. there is not enough of a certain enzyme which is needed to metabolize a type of fat called long-chain fatty acids. The build-up of these fatty acids in the body causes damage. There are three subtypes of the disorder each with varying severity: severe early-onset form, an intermediate form and an adult-onset form. The intermediate form is relatively mild and tends to be characterized by periods of low blood sugar - symptoms tend to develop during childhood.
• Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency: A rare inherited genetic condition where the body is unable to convert certain fats to energy i.e. there is not enough of a certain enzyme which is needed to metabolize a type of fat called long-chain fatty acids. The build-up of these fatty acids in the body causes damage. There are three subtypes of the disorder each with varying severity: severe early-onset form, an intermediate form and an adult-onset form.
• Vibrio infection - Vibrio alginolyticus: An infectious disease caused by a bacteria called Vibrio alginolyticus. This bacterium tends to cause ear and wound infections.
• Vibrio infection - Vibrio cincinnatiensis: An infectious disease caused by a bacteria called Vibrio cincinnatiensis. The nature and severity of symptoms can vary considerably depending on the type of infection caused - gastroenteritis, wound infection or septicemia. This particular infection however tends to cause mainly meningitis. The elderly and very young tend to suffer more severe symptoms.
• Vibrio infection - Vibrio damsela: An infectious disease caused by a bacteria called Vibrio damsela. The nature and severity of symptoms can vary considerably depending on the type of infection caused - gastroenteritis, wound infection or septicemia. Wound infection is the most common disease associated with this bacteria and septicemia and gastroenteritis is relatively rare. Infection usually occurs through consumption of contaminated seafood or exposure of a wound to contaminated water. The elderly and very young tend to suffer more severe symptoms.
• Vibrio infection - Vibrio fluvialis: An infectious disease caused by a bacteria called Vibrio fluvialis. The nature and severity of symptoms can vary considerably depending on the type of infection caused - gastroenteritis, wound infection or septicemia. Gastroenteritis is the most common disease associated with this bacteria and septicemia is relatively rare. Infection usually occurs through consumption of contaminated seafood or exposure of a wound to contaminated water. The elderly and very young tend to suffer more severe symptoms.
• Vibrio infection - Vibrio furnissii: An infectious disease caused by a bacteria called Vibrio furnissii. The nature and severity of symptoms can vary considerably depending on the type of infection caused - gastroenteritis, wound infection or septicemia. Gastroenteritis is the most common disease associated with this bacteria and septicemia and wound infection is relatively rare. Infection usually occurs through consumption of contaminated seafood or exposure of a wound to contaminated water. The elderly and very young tend to suffer more severe symptoms.
• Vibrio infection - Vibrio holisae: An infectious disease caused by a bacteria called Vibrio holisae. The nature and severity of symptoms can vary considerably depending on the type of infection caused - gastroenteritis, wound infection or septicemia. Gastroenteritis is the most common disease associated with this bacteria and septicemia is relatively rare. Infection usually occurs through consumption of contaminated seafood or exposure of a wound to contaminated water. The elderly and very young tend to suffer more severe symptoms.
• Vibrio infection - Vibrio metschnikovii: An infectious disease caused by a bacteria called Vibrio metschnikovii. The nature and severity of symptoms can vary considerably depending on the type of infection caused - gastroenteritis, wound infection or septicemia. Gastroenteritis is the most common disease associated with this bacteria and septicemia is relatively rare. Infection usually occurs through consumption of contaminated seafood or exposure of a wound to contaminated water. The elderly and very young tend to suffer more severe symptoms.
• Vibrio infection - Vibrio mimicus: An infectious disease caused by a bacteria called Vibrio mimicus. The nature and severity of symptoms can vary considerably depending on the type of infection caused - gastroenteritis, wound infection or septicemia. Gastroenteritis is the most common disease associated with this bacteria and septicemia and wound infection is relatively rare. Infection usually occurs through consumption of contaminated seafood or exposure of a wound to contaminated water. The elderly and very young tend to suffer more severe symptoms.
• Vibrio infection - Vibrio parahaemolyticus: An infectious disease caused by a bacteria called Vibrio parahaemolyticus. The nature and severity of symptoms can vary considerably depending on the type of infection caused - gastroenteritis, wound infection or septicemia. Gastroenteritis is the most common disease associated with this bacteria and septicemia is relatively rare. Infection usually occurs through consumption of contaminated seafood or exposure of a wound to contaminated water. The elderly and very young tend to suffer more severe symptoms.
• Vibrio infections: Infection by a bacteria which occurs naturally in seawater and in the stomach of many seawater animals. It is a serious infection and accounts for most seafood-related deaths. It causes severe gastrointestinal symptoms and can also cause wound infection.
• Vibrio vulnificus: Bacteria commonly infecting oysters and seafood.
• Vipoma: A rare disorder caused by an increase in secretion of vasoactive intestinal peptide by the pancreas. The syndrome is often caused by an islet-cell tumor (except for beta cells) in the pancreas.
• Viral pericarditis: Inflammation and swelling of the pericardium (fibrous sac surrounding the heart) that results from a viral infection. Causative viruses include HIV, coxsackieviruses, echoviruses and adenoviruses. The condition may be misdiagnosed as a heart attack and vice versa.
• Virilizing ovarian tumor: An ovarian tumor made up of hormone secreting cells which results in excessive male hormone (androgen) production.
• Virus-induced asthma: Virus-induced asthma refers to inflammation and constriction of the airways that is triggered by a viral respiratory infection. This form of asthma usually has a sudden onset and is relatively severe. Viral respiratory infections can also exacerbate existing asthma symptoms.
• Visceral leishmaniasis (kala-azar): A rare infectious disease caused by any of a number of parasitic Leishmania species. Infection can cause any of three different manifestations: cutaneous leishmaniasis, mucosal leishmaniasis and visceral leishmaniasis. Visceral leishmaniasis infection involves the spleen, liver and bone marrow and can be fatal if untreated.
• Visceral steatosis: An inherited condition characterized by the deposition of small papules composing of granulomas in organs of the body.
• Vocal cord carcinoma: A cancer that occurs in the vocal cords. Predisposing factors for this type of cancer include smoking, chemicals, environmental irritants and metabolic problems.
• Vocal cord dysfunction familial: A rare inherited disorder where the vocal cord closes while breathing in which causes breathing difficulty which can be severe in some cases. Mental retardation is also associated.
• Vocal papilloma: A common harmless bump that develops near the glottal closure and affects voice quality. The bump or tumor is caused by a papovavirus infection of the throat.
• Volak rodenticide poisoning: Volak is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Volid rodenticide poisoning: Volid is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
• Vulva symptoms: Symptoms related to the vulva (external skin region near vagina)
• Vulvar neoplasms: A tumor that develops in the tissue of the vulva.
• Walrus poisoning: The walrus is used as a food source in some parts of the world. Eating the liver of the walrus can result in a Vitamin A overdose which can cause serious symptoms and even death in extreme cases.
• Warm Autoimmune Hemolytic Anemia: Warm autoimmune hemolytic anemia is a condition where the body's immune system triggers the production of antibodies against the body's own red blood cells. The red cells are destroyed at an abnormally rapid rate which leads to anemia. Warm haemolytic anemia is characterized by the fact that the abnormal destruction of red blood cells is more active when the patient is exposed to warm temperatures. The severity of the condition varies depending on the underlying cause e.g. cytomegalovirus, hepatitis, HIV and lupus. The condition may develop gradually or occur suddenly and cause serious symptoms.
• Water-skier colon: Injury caused by the entry of water at high speed into the rectum or vagina which can occur in high-speed water-skiing. Some cases can be severe enough to cause internal lacerations which can result in death due to blood loss if left untreated. Injury can be avoided by wearing reinforced skiing apparel rather than simply swimwear.
• Waterhouse-Friederichsen syndrome: A rare syndrome that occurs as complication of septicemia (often due to meningococcal or pneumococcal infection) and involves blood coagulation in blood vessels, adrenal gland hemorrhages and ultimately kidney failure.
• Weil's syndrome: Severe form of Leptospirosis
• Wernicke-Korsakoff syndrome: A rare degenerative brain disorder caused by thiamine (Vitamin B1) deficiency. Chronic alcoholics are prone to this condition.
• Western equine encephalitis: An infectious disease caused by an arbovirus (Alphavirus - Togaviraidae) and transmitted by infected mosquitoes. The infection primarily attacks that central nervous system and severity can range from asymptomatic to severe complications and even death in rare cases.
• Whipple's Disease: Rare malabsorption disease from bacterial digestive infection
• White Chameleon poisoning: The white chameleon is a type of thistle found mainly in dry areas of the Mediterranean. The rhizomes contains chemicals which can cause poisoning symptoms if eaten. The plant is often mistaken for a wild artichoke. The root extract is sometimes used in alternative medicine and excessive doses can also result in poisoning.
• White snakeroot poisoning: White snakeroot is a herbaceous plant which is found mainly growing in the wild in the US and has round clusters of small white flowers. The plant contains a chemical called tremetol which can cause gastrointestinal symptoms in people who drink the raw milk or eat the meat from cows who have fed on the plant. The plant itself is considered very poisonous to humans and eating the plant can result in death.
• White whale poisoning: The White whale is used as a food source in the Arctic. The white whale may cause toxicity if the meat and visceral organs eaten by humans in sufficient quantities.
• Whooping Cough: An infectious condition caused by the bacteria Bordetella pertussis
• Wild Lima bean poisoning: Wild Lima beans are a legume similar to the common lima beans which are considered safe to eat. The wild lima contains much higher levels of a chemical called cyanogen than the common lima bean. The cyanogen can cause symptoms and if sufficient quantities are eaten, death can result. Some people are so sensitive to cyanogen that eating even the relatively safe common lima bean may result in symptoms though usually they are not severe. Cooking destroys the toxic chemical in lima beans. Raw lima bean sprouts should be avoided.
• Wild cherry seed poisoning: Wild cherry seeds contain a chemical called amygdalin which breaks down into cyanide in the human body. The toxic chemicals are not released if the seed remains intact and therefore poisoning usually only occurs if the seeds are crushed and eaten. Accidental ingestion is very unusual.
• Wilms tumor 2: A familial form malignant kidney tumor that occurs in children. Type 2 differs from other forms of Wilms tumor by the origin of the genetic defect (chromosome 11p15.5).
• Wilms tumor 3: A dominantly inherited form malignant kidney tumor that occurs in children. Type 3 differs from other forms of Wilms tumor by the origin of the genetic defect (chromosome 16q).
• Wilms tumor 4: A familial form malignant kidney tumor that occurs in children. Type 4 differs from other forms of Wilms tumor by the origin of the genetic defect (chromosome 17q12-q21).
• Wilms tumor and radial bilateral aplasia: A condition that is characterised by bilateral aplasia of the kidneys and wilms tumor
• Wilson's disease: Wilson disease, or hepatolenticular degeneration, is a neurodegenerative disease of copper metabolism.
• Wolfram's disease: A condition that is inherited and consists of multiple symptoms
• Wolman disease: A rare inherited lipid storage disease. The condition usually results in death early in life.
• Wounds, Stab: Wounds caused by a sharp implement. The injury may be accidental or self-inflicted. Symptoms depend on the size, depth and location of the stab wound. The severing of a major blood vessel can rapidly lead to death.
• Xanthid crab poisoning (Palytoxin): Palytoxin is a marine toxin found in some xanthid crabs from the Philippines and Singapore region. The toxin is extremely potent and death is common in patients who ingest contaminated xanthid crabs.
• Xanthomatosis cerebrotendinous: A rare inherited condition where cholesterol is deposited in the brain and other parts of the body. The disease is classified as a lipid storage disorder due to the abnormal deposition of cholesterol and cholestanol in various parts of the body - especially the brain, lungs and Achilles tendon. The condition is possibly highly underdiagnosed.
• Yellow fever: A viral infection transmitted by mosquito bites which can damage various organs such as the liver, heart, kidney and digestive tract.
• Yellow jessamine poisoning: The Yellow Jessamine is a woody vine which bears aromatic, funnel-shaped yellow flowers and flat fruit capsules. The plant contains alkaloids which are very toxic and potentially fatal if eaten in sufficient quantities.
• Yellow pleated parasol poisoning: Yellow pleated parasol is a bright yellow, bell-shaped mushroom with a yellow powdery substance over the cap. The mushroom is very poisonous and death can result if sufficient quantities are eaten. However, most cases result in gastrointestinal symptoms only.
• Young McKeever Squier syndrome: A condition that affects the olivopontocerebellum and the cerebellar cortex of the brain
• Young syndrome: Symptoms in a fetus that occur when the mother is suffering from advanced diabetes mellitus during pregnancy.
• Yunis Varon syndrome: A multisystem genetic disease that affects the skeletal system in particular
• Zinc deficiency: When there is a deficiency of zinc in an individuals body
• Zygomycosis: An infectious disease caused by fungus from the orders Mucorales and Entomophthorales which are normally found in the soil and in decaying plant matter. The infection differs from mucormycosis which only involves the order Mucorales. Transmission is usually through the inhalation of spores. It is generally harmless to healthy individuals but can cause infection in patients who are immunocompromised or who have a serious chronic illness such as uncontrolled diabetes. Symptoms and severity can vary considerable depending on the part of the body the infection occurs in - gastrointestinal tract, skin, lungs, central nervous system, eye orbit and the paranasal sinuses.

Rate This Website

What do you think about the features of this website? Take our user survey and have your say:

Website User Survey

Medical Tools & Articles:

Next articles:

• Disease Center Information
• Surveys
• Join in at the forums

Tools & Services:

• Bookmark this page
• Surveys relating to Death
• Symptom Search
• Symptom Checker
• Medical Dictionary
• Give your feedback

Medical Articles:

• Disease & Treatments Search
• Misdiagnosis Center
• Full list of interesting articles

Forums & Message Boards

• Ask or answer a question at the Boards:
• I cannot get a diagnosis. Please help.
• Tell us your medical story.
• Share your misdiagnosis story.
• What is the best treatment for my condition?
• See all the Boards.

Enter your search terms Submit search form
Search The Web Search wrongdiagnosis.com

Common Health Mistakes

Symptom
Checker

Search Specialists by State and City