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Wolfram syndrome
Introduction: Wolfram syndrome
Description of Wolfram syndrome
Wolfram syndrome (medical condition):
A condition that is inherited and consists of multiple symptoms.
See also Wolfram's disease:
»Introduction: Wolfram's disease
»Symptoms of Wolfram's disease
Wolfram syndrome: A hereditary condition characterized by multiple symptoms including those of DIABETES INSIPIDUS; DIABETES MELLITUS; OPTIC ATROPHY; and DEAFNESS. This syndrome is also known as DIDMOAD (first letter of each word) and is usually associated with VASOPRESSIN deficiency. It is caused by mutations in gene WFS1 encoding wolframin, a 100-kDa transmembrane protein.
Source: MeSH 2007
Wolfram syndrome: Rare Disease
Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)
Wolfram syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Wolfram syndrome, or a subtype of Wolfram syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Wolfram syndrome as a Disease
Wolfram syndrome: Another name for Wolfram's disease (or close medical condition association).
»Introduction: Wolfram's disease
»Symptoms of Wolfram's disease
Symptoms of Wolfram syndrome (Wolfram's disease)
Some of the symptoms of Wolfram syndrome incude:
- Anxiety
- Emotional liability
- Depression
- Hypotonia
- Impaired problem solving
See full list of 45 symptoms of Wolfram syndrome (Wolfram's disease)
Terms associated with Wolfram syndrome:
Terms Similar to Wolfram syndrome:
Source - NIH
Source - MeSH 2007
Broader terms for Wolfram syndrome
Source - MeSH 2007
The following terms can be used for Wolfram syndrome
Source: CRISP
Hierarchical classifications of Wolfram syndrome
The following list attempts to classify Wolfram syndrome into categories where each line is subset of the next.
MeSH 2007 Hierarchy:
MeSH 2007 Hierarchy
MeSH 2007 Hierarchy
MeSH 2007 Hierarchy
MeSH 2007 Hierarchy
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