Misdiagnosis of Hidden Causes of Cleft palate

Other underlying conditions related to Cleft palate:

• Feeding problem of newborn

Source: Diseases Database

Cleft palate as a complication:

Other conditions that might have Cleft palate as a complication might be potential underlying conditions. The list of conditions listing Cleft palate as a complication includes:

• Folate deficiency
• Velocardiofacial syndrome

Cleft palate Causes: Book Excerpts

• Differential Diagnosis - Cleft Lip/Palate
• Causes and incidence - Cleft lip and cleft palate
• Causes - Cleft lip and cleft palate

Cleft palate as a symptom:

Conditions listing Cleft palate as a symptom may also be potential underlying conditions.

For a more detailed analysis of Cleft palate as a symptom, including causes, drug side effect causes, and drug interaction causes, please see our Symptom Center information for Cleft palate.

• 11q Partial Trisomy
• 14q+ syndrome
• 18p minus syndrome
• 1q deletion
• 22q11.2 deletion syndrome
• 2q deletion
• 2q22-q24 deletion
• 3q deletion
• 4p16.3 deletion
• Aase-Smith I syndrome
• Abruzzo Erickson syndrome
• Accutane - Teratogenic Agent
• Achard syndrome
• Achondrogenesis
• Acrocallosal Syndrome (Schinzel Type)
• Acrofacial dysostosis atypical postaxial
• Acrofacial dysostosis autosomal recessive
• Acrofacial dysostosis postaxial, atypical
• Acrofacial dysostosis Preis type
• Acrofacial dysostosis, Nager type
• Acrofrontofacionasal dysostosis syndrome
• Acrosphenosyndactylia
• Acyclovir - Teratogenic Agent
• Adducted thumb syndrome recessive form
• Adducted thumbs - arthrogryposis, Christian type
• Aflatoxin B1- Teratogenic Agent
• Agammaglobulinemia - microcephaly - craniosynostosis - severe dermatitis
• Agammaglobulinemia, microcephaly, and severe dermatitis
• Alopecia, anosmia, deafness, hypogonadism syndrome
• Aminopterin - Teratogenic Agent
• Amphetamines - Teratogenic Agent
• André syndrome
• Ankyloblepharon filiforme adnatum - cleft palate
• Anophthalmia - cleft palate - micrognathia
• Anophthalmia - hypothalamo-pituitary insufficiency
• Anophthalmia - hypyothalamo-pituitary insufficiency
• Anophthalmia cleft lip palate hypothalamic disorder
• Anophthalmia plus syndrome
• Anotia - facial palsy - cardiac defect
• Apelt-Gerkin-Lenz Syndrome
• Apert syndrome
• Arthrogryposis distal type II
• Atelosteogenesis Type III
• Atelosteogenesis, type 2
• Atorvastatin - Teratogenic Agent
• Aughton syndrome
• Auricular abnormalities - cleft lip with or without cleft palate - ocular abnormalities
• Auriculo-condylar syndrome
• Auriculoocular anomalies - cleft lip
• Autosomal Recessive Tetra-Amelia
• Axenfeld-Rieger syndrome
• Axial mesodermal dysplasia spectrum
• Bamforth syndrome
• Baraitser-Rodeck-Garner syndrome
• Bartsocas Papa syndrome
• BBB syndrome, X-linked
• Beare-Stevenson cutis gyrata syndrome
• Berndorfer syndrome
• Bixler-Christian-Gorlin syndrome
• Blepharo facio skeletal syndrome
• Blepharoptosis - cleft palate - ectrodactyly - dental anomalies
• Brachio-Skeletal-Genital Syndrome
• Brachioskeletogenital syndrome
• Brachycephaly - deafness - cataract - mental retardation
• Brachycephaly - deafness - cataract - microstomia - mental retardation
• C-like syndrome
• Camera-Marugo-Cohen syndrome
• Campomelia Cumming type
• Campomelic dwarfism
• Campomelic dysplasia
• Camptomelic dysplasia I
• Camptomelic dysplasia II
• Cardiac malformation, cleft lip-palate, microcephaly and digital anomalies
• CATCH 22
• Catel-Manzke Syndrome
• Cerebro-facio-thoracic dysplasia
• Cervenka's syndrome
• CHARGE Syndrome
• Charlie M syndrome
• Cholestasis - pigmentary retinopathy - cleft palate
• Chondrodysplasia, type Nance-Sweeney
• Christian's syndrome 1
• Chromosome 1, 1p36 deletion syndrome
• Chromosome 1, deletion q21 q25
• Chromosome 1, duplication 1p21 p32
• Chromosome 1, monosomy 1q32 q42
• Chromosome 1, monosomy 1q4
• Chromosome 1, Partial Trisomy
• Chromosome 1, pter-p36
• Chromosome 1, uniparental disomy 1q12 q21
• Chromosome 10, distal trisomy 10q
• Chromosome 10, trisomy 10p
• Chromosome 10p deletion syndrome
• Chromosome 10p duplication syndrome
• Chromosome 10p duplication/10q deletion syndrome
• Chromosome 10p terminal deletion syndrome
• Chromosome 11, Partial Trisomy 11q
• Chromosome 11q duplication syndrome
• Chromosome 12 trisomy
• Chromosome 12, 12p trisomy
• Chromosome 12, Isochromosome 12p Mosaic
• Chromosome 12p duplication syndrome
• Chromosome 12p tetrasomy syndrome
• Chromosome 13 ring syndrome
• Chromosome 13 trisomy syndrome
• Chromosome 13p duplication
• Chromosome 13q deletion
• Chromosome 13q deletion syndrome
• Chromosome 13q duplication syndrome
• Chromosome 14 trisomy
• Chromosome 14 trisomy syndrome
• Chromosome 14, trisomy mosaic
• Chromosome 14q, proximal duplication
• Chromosome 15 trisomy
• Chromosome 15q duplication syndrome
• Chromosome 15q, partial duplication (unbalanced translocation)
• Chromosome 15q, trisomy
• Chromosome 16p, partial duplication
• Chromosome 16q, partial duplication
• Chromosome 17, deletion 17q23 q24
• Chromosome 17p, partial deletion
• Chromosome 17q, partial duplication
• Chromosome 18 mosaic monosomy
• Chromosome 18, Tetrasomy 18p
• Chromosome 18q, partial deletion
• Chromosome 19q, partial duplication
• Chromosome 1p deletion syndrome
• Chromosome 1p duplication syndrome
• Chromosome 1q deletion
• Chromosome 1q duplication syndrome
• Chromosome 2 trisomy syndrome
• Chromosome 2, monosomy 2q
• Chromosome 21 monosomy
• Chromosome 21q deletion syndrome
• Chromosome 22 Ring
• Chromosome 22 trisomy mosaic
• Chromosome 22, microdeletion 22q11
• Chromosome 22, trisomy
• Chromosome 22q deletion
• Chromosome 22q deletion syndrome
• Chromosome 22q duplication syndrome
• Chromosome 22q11 deletion
• Chromosome 22q11.2 deletion syndrome
• Chromosome 22q11.2 microduplication
• Chromosome 3, trisomy 3p
• Chromosome 3, trisomy 3q
• Chromosome 3/B translocation
• Chromosome 4 ring syndrome
• Chromosome 4 short arm deletion
• Chromosome 4, Monosomy 4q
• Chromosome 4p deletion syndrome
• Chromosome 6, monosomy 6q
• Chromosome 6, partial trisomy 6q
• Chromosome 6, trisomy 6q
• Chromosome 6q deletion syndrome
• Chromosome 6q duplication syndrome
• Chromosome 7 deletion p15.1-p21.1
• Chromosome 7 ring syndrome
• Chromosome 7, Partial Deletion of Short Arm
• Chromosome 7, partial monosomy 7p
• Chromosome 7, trisomy 7p
• Chromosome 7, trisomy 7q
• Chromosome 7p deletion syndrome
• Chromosome 7p duplication syndrome
• Chromosome 7q duplication syndrome
• Chromosome 7q partial deletion
• Chromosome 8 recombinant syndrome
• Chromosome 8 trisomy syndrome
• Chromosome 8, mosaic trisomy
• Chromosome 8, partial trisomy
• Chromosome 8, trisomy
• Chromosome 9 trisomy syndrome
• Chromosome 9, trisomy
• Chromosome 9, Trisomy 9p (Multiple Variants)
• Chromosome 9, trisomy 9q
• Chromosome 9/mosaic
• Chromosome 9p tetrasomy syndrome
• Chromosome 9q duplication
• Chromosome 9q duplication syndrome
• Chromosomes 1 and 2, monosomy 2q duplication 1p
• Cleft lip - palate - abnormal thumbs - microcephaly
• Cleft lip - palate - ectrodactyly
• Cleft lip - palate - mental retardation - corneal opacity
• Cleft lip and palate - malrotation - cardiopathy
• Cleft lip palate - oligodontia - syndactyly - pili torti
• Cleft lip palate incisor and finger anomalies
• Cleft lip palate pituitary deficiency
• Cleft lip with or without cleft palate
• Cleft palate - cardiac defect - genital anomalies - ectrodactyly
• Cleft palate - coloboma - deafness
• Cleft palate - heart disease - polydactyly - absent tibia
• Cleft palate - lateral synechia syndrome
• Cleft palate - short stature - vertebral anomalies
• Cleft palate - stapes fixation - oligodontia
• Cleft Palate and Cleft Lip
• Cleft palate cardiac defect ectrodactyly
• Cleft palate colobomata radial synostosis deafness
• Cleft palate, bilateral choanal atresia, curly hair and congenital hypothyroidism
• Cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss
• Cleft palate, X-linked
• Clefting - ectropion - conical teeth
• Collagenopathy, type 2 alpha 1
• Coloboma of macula, type B brachydactyly
• Coloboma uveal with cleft lip palate and mental retardation
• Coloboma, cleft lip/palate and mental retardation syndrome
• Complete Trisomy 18 syndrome
• Congenital Diarrhea, Secretory Sodium, Syndromic, 3
• Conotruncal heart malformations
• Contractures - ectodermal dysplasia - cleft lip palate
• Contractures, congenital, torticollis and malignant hyperthermia
• Cornelia de Lange Syndrome
• Cornelia de Lange syndrome 1
• Cornelia de Lange syndrome 2
• Corpus callosum agenesis - blepharophimosis - Robin sequence
• Corpus callosum, agenesis of, blepharophimosis Robin type
• Crane-Heise syndrome
• Craniofrontonasal dysplasia
• Craniomicromelic syndrome
• Craniosynostosis - brachysyndactyly of hands and absence of toes
• Craniosynostosis arthrogryposis cleft palate
• Craniosynostosis cleft lip palate arthrogryposis
• Craniosynostosis Maroteaux Fonfria type
• Craniosynostosis mental retardation clefting syndrome
• Cri-du-chat syndrome
• Crumpled helices and small mouth
• Cystic hygroma, lethal - cleft palate
• Czeizel syndrome
• Del(1) (23-q25)
• Del(1) (q12-q21.3)
• Del(1) (q25-q32)
• Del(1) (q32-q41)
• Del(1) (q41-q43)
• Del(1) (q41-qter)
• Del(1) (q43-qter) & dup (22) (pter-q13)
• Deletion 10pter
• Deletion 13q
• Deletion 22q11
• Deletion 2q
• Deletion 4p
• Deletion 5p
• Deletion 6q
• Desbuquois dysplasia
• Desmosterolosis
• Dextrocardia - microphthalmia - cleft palate - intellectual deficit
• Diaphanospondylodysostosis
• DiGeorge syndrome
• Dilantin - Teratogenic Agent
• Dincsoy-Salih-Patel syndrome
• Diprosopia
• Distal Trisomy 11q
• Distal trisomy 6q
• Distinctive Craniofacial Features - Pterygia - Mental Retardation
• Dup (1) (q23-qter) and del (3)(pter-p25)
• Dup (1)(pter-p31) and del(2)(q33-qter)
• Dup(1) (p31-p11)
• Dup(1) (p31-p21)
• Dup(1) (p35-p31)
• Dup(1) (q24-q31.2)
• Duplication 10p
• Duplication 12p
• Duplication 13
• Duplication 18
• Duplication 6q
• Duplication 6q, partial
• Duplication 7p
• Duplication 7q
• Dysgnathia complex
• Dysmorphism - cleft palate - loose skin
• Dysraphism - cleft lip palate - limb reduction defects
• ECP syndrome
• Ectodermal dysplasia - mental retardation - CNS malformation
• Ectodermal dysplasia, hypohidrotic, autosomal dominant
• Ectodermal dysplasia, Margarita type
• Ectrodactyly - Ectodermal Dysplasia - Cleft Lip/Palate Syndrome, Type 1
• Ectrodactyly - Ectodermal Dysplasia - Cleft Lip/Palate Syndrome, Type 3
• Ectrodactyly cleft palate syndrome
• Ectrodactyly-ectodermal dysplasia-cleft lip/cleft palate
• Edward Syndrome
• Edwards Syndrome
• Elliott-Ludman-Teebi syndrome
• Ellis-Yale-Winter syndrome
• Emanuel syndrome
• Engelhard-Yatziv syndrome
• Erythromycin - Teratogenic Agent
• Eye defects - arachnodactyly - cardiopathy
• Facial clefting corpus callosum agenesis
• Faciocardiorenal syndrome
• Familial Treacher Collins syndrome
• Femoral facial syndrome
• Fernhoff-Blackston-Oakley syndrome
• Fetal alcohol syndrome
• Fetal Hydantoin Syndrome
• Fibrochondrogenesis
• Filippi Syndrome
• Fine-Lubinsky syndrome
• Foramina parietalia permagna
• Franceschetti-Klein syndrome
• Franceschini-Vardeu-Guala syndrome
• Fraser Syndrome
• Fraser-like syndrome
• Fronto-facio-nasal dysplasia
• Frontofacionasal dysplasia type Al gazali
• Frontonasal dysplasia
• Froster-Iskenius-Waterson syndrome
• Fryns Syndrome
• Furlong-Kurczynski-Hennessy syndrome
• Genée-Wiedemann syndrome
• German syndrome
• Gollop syndrome
• Gonadal dysgenesis XY type associated anomalies
• Gordon Syndrome
• Grix-Blankenship-Peterson syndrome
• Grob syndrome
• Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate
• Growth delay - mental retardation - mandibulofacial dysostosis - microcephaly - cleft palate
• Hajdu-Cheney Syndrome
• Halal syndrome
• Hanhart syndrome type III
• Hardikar syndrome
• Harper dwarfism
• Haspeslagh Fryns Muelenaere syndrome
• Hay-Wells Syndrome
• Hay-Wells syndrome, recessive type
• Herrmann Opitz arthrogryposis syndrome
• Herrmann-Opitz craniosynostosi
• Hirschsprung - microcephaly - cleft palate
• Ho Kaufman-Mcalister syndrome
• Holoprosencephaly - caudal dysgenesis
• Holoprosencephaly - ectrodactyly - cleft lip/palate
• Holoprosencephaly deletion 2p
• Holzgreve-Wagner-Rehder syndrome
• Howard-Young syndrome
• Hunter-Carpenter-Macdonald syndrome
• Hurst-Hallam-Hockey syndrome
• Hydrolethalus syndrome
• Hypertelorism - esophageal abnormalities - hypospadias
• Hypertelorism with esophageal abnormality and hypospadias
• Hyperthermia induced defects
• Hypomandibular faciocranial dysostosis
• Hypomelanosis of Ito
• Hypopituitarism - micropenis - cleft lip palate
• Hypospadias - hypertelorism
• Hypotelorism - cleft palate - hypospadias
• Hypothyroidism - cleft palate
• Hypothyroidism - dermoid cyst - cleft palate
• Iida-Kannari syndrome
• Imaizumi Kuroki syndrome
• Incontinentia Pigmenti
• Iniencephaly
• Isotretinoin embryopathy like syndrome
• Johnson-Hall-Krous syndrome
• Jones-Hersh-Yusk syndrome
• Joubert Syndrome
• Juberg-Hayward syndrome
• Juvenile-onset dystonia
• Kabuki syndrome
• Kallmann Syndrome
• Kaplan-Plauchu-Fitch syndrome
• Kapur-Toriello syndrome
• Klippel Feil deformity conductive deafness absent vagina
• Klippel Feil Syndrome
• Klippel-Feil syndrome recessive type
• Klippel-Feil syndrome, dominant type
• Kniest dysplasia
• Korula-Wilson-Salomonson syndrome
• Krieble Bixler syndrome
• Kunze riehm syndrome
• Kuster syndrome
• Lamotrigine - Teratogenic Agent
• Larsen syndrome
• Larsen syndrome, dominant type
• Larsen syndrome, recessive type
• Larsen-like syndrome, lethal form
• Larsen-like syndrome, lethal type
• Lathosterolosis
• Lethal chondrodysplasia, Moerman type
• Limb-mammary syndrome
• Loeys-Dietz syndrome
• Lowry syndrome
• Lowry-Maclean syndrome
• Lymphoedema - cleft palate
• Macrosomia with lethal microphthalmia
• Mandibulofacial dysostosis, Treacher Collins type, autosomal recessive
• Marden-Walker Syndrome
• Marden-Walker-like syndrome
• Mayer-Rokitansky-Kuster-Hauser, syndrome, type 2 (MRKH type 2)
• McGillivray syndrome
• Meckel Syndrome
• Meckel syndrome, type 5
• Mefloquine - Teratogenic Agent
• Meningeal angiomatosis - cleft hypoplastic left heart
• Mental retardation - hypotonic facies syndrome, X-linked, 1
• Mental Retardation - Pterygia - Shortness - Distinctive Facial Appearance
• Mental retardation - short stature - cleft palate - unusual facies
• Mental retardation - short stature - deafness - genital
• Mental retardation, Smith-Fineman-Myers type
• Mental retardation, Wolff type
• Mental retardation, X-linked, Armfield type
• Mental retardation, X-linked, Reish type
• Mental retardation, X-linked, Siderius type
• Methotrexate - Teratogenic Agent
• Michelin Tire Baby Syndrome
• Michelin tyre baby syndrome
• Microcephaly - facial clefting - preaxial polydactyly
• Microcephaly - microphthalmia - ectrodactyly of lower limbs - prognathism
• Microcephaly immunodeficiency lymphoreticuloma
• Microcephaly, corpus callosum dysgenesis and cleft lip-palate
• Microphthalmia syndromic, type 8
• Microphthalmia syndromic, type 9
• Microsomia - hemifacial - radial defects
• Midline craniofacial anomalies and morning glory disc anomaly
• Midline field defects
• Mobius syndrome
• Monosomy 18 Mosaic
• Monosomy 18 mosaicism
• Monosomy 1p36
• Mowat-Wilson syndrome
• Moynahan syndrome III
• Mucopolysaccharidosis, type 9
• Mullerian Aplasia - Renal Aplasia - Cervicothoracic Somite Dysplasia
• Multiple Benign Ring-Shaped Creases on Limbs
• Multiple congenital anomalies - mental retardation - growth failure and cleft lip/ palate
• Multiple pterygium syndrome
• Multiple pterygium syndrome lethal type
• Multiple pterygium syndrome, autosomal recessive
• MURCS Association
• Möbius syndrome
• Nasopharyngeal teratoma with Dandy-Walker - diaphragmatic hernia
• Native American myopathy
• Neomycin - Teratogenic Agent
• Nijmegen Breakage Syndrome
• Oculo cerebro acral syndrome
• Oculofaciocardiodental syndrome
• Oculomaxillofacial dysostosis
• Oculopalatocerebral syndrome
• Oculopalatoskeletal syndrome
• Okamuto Satomura syndrome
• Opitz G Syndrome
• Opitz G/BBB Syndrome
• Opitz G/BBB syndrome, Autosomal dominant
• Opitz G/BBB Syndrome, type I
• Opitz G/BBB Syndrome, Type II
• Opitz G/BBB Syndrome, X-linked
• Opitz syndrome
• Opitz syndrome , X-linked
• Oral facial digital syndrome, type 4
• Oral-facial cleft
• Orofaciodigital syndrome type1
• Orofaciodigital syndrome, Gabrielli type
• Orofaciodigital syndrome, Shashi type
• Oromandibular-limb hypogenesis spectrum
• OSMED, Homozygous
• Osteogenesis imperfecta, type 2
• Osteogenesis imperfecta, type 2A
• Osteogenesis imperfecta, type IIB
• Osteopathia striata, cranial sclerosis
• Oto-Palatal-digital syndrome
• Oto-palato-digital syndrome, type 2
• Oto-spondylo-megaepiphyseal dysplasia, autosomal recessive
• Oto-spondylo-megaepiphyseal dysplasia, homozygous
• Otopalatodigital Syndrome Type I
• Otopalatodigital Syndrome Type I and II
• Otospondylomegaepiphyseal dysplasia
• Palant cleft palate syndrome
• Pallister Killian Mosaic Syndrome
• Pallister Mosaic Syndrome Tetrasomy 12p
• PARC syndrome
• Partial 7p Monosomy
• Partial Trisomy 18 Syndrome
• Partial Trisomy 3pter
• Patau syndrome
• Pena Shokeir syndrome, type 1
• Periodic paralysis, potassium-sensitive, cardiodysrythmic type
• Pfeiffer syndrome Type 2
• Phendimetrazine - Teratogenic Agent
• Phenytoin - Teratogenic Agent
• Phillips-Griffiths syndrome
• Pierre Robin sequence with pectus excavatum and rib and scapular anomalies
• Pilotto syndrome
• Polydactyly cleft lip palate psychomotor retardation
• Polydactyly visceral anomalies cleft lip palate
• Popliteal pterygium syndrome
• Popliteal pterygium syndrome, lethal type
• Pseudoaminopterin syndrome
• Pseudodiastrophic dysplasia
• Pseudotrisomy 13 syndrome
• Pterygia - Mental retardation - Distinctive Craniofacial Features
• Pterygium, Popliteal, lethal type
• Radial defect - Robin sequence
• Raine syndrome
• Ranitidine - Teratogenic Agent
• Rapadilino syndrome
• Rapp-Hodgkin syndrome
• Reardon-Hall-Slaney syndrome
• Reese-Ellsworth syndrome
• Retention of tears - ectrodactyly - ectodermal dysplasia - strange hair, skin and teeth
• Rhizomelic syndrome
• Richieri Costa Guion-Almeida syndrome
• Richieri-Costa-Orquizas syndrome
• Richieri-Costa-Silveira-Pereira syndrome
• Rieger Syndrome
• Roberts-SC Phocomelia
• Rolland-Desbuquois syndrome
• Samson-Viljoen syndrome
• Say syndrome
• Schisis association
• Schneckenbecken dysplasia
• Schrander-Stumpel, Theunissen, Hulsmans syndrome
• Septo-Optic Dysplasia
• Short limb dwarf lethal, Mcalister Crane type
• Short limbs subluxed knees cleft palate
• Short rib-polydactyly syndrome, Majewski type
• Short stature - craniofacial anomalies - genital hypoplasia
• Short stature - monodactylous - ectrodactyly - cleft palate
• Shprintzen syndorme
• Siderius type X-linked mental retardation syndrome
• Silverman-Handmaker syndrome
• Simpson-Golabi-Behmel syndrome, type 1 (SGBS1)
• Simpson-Golabi-Behmel syndrome, type 2
• Single upper central incisor
• Skeletal dysplasia - mental retardation
• Skin Creases, Multiple Benign Ring-Shaped, of Limbs
• Smith-Fineman-Myers syndrome 1
• Smith-Lemli-Opitz syndrome, type 2
• Snyder-Robinson syndrome
• Spondylocostal dysostosis, Dandy-Walker
• Spondyloepimetaphyseal dysplasia joint laxity
• Spondyloepimetaphyseal dysplasia with joint laxity
• Spondyloepiphyseal dysplasia, congenita
• Steinfeld syndrome
• Stevenson-Carey syndrome
• Streptomycin - Teratogenic Agent
• Syngnathia - cleft palate
• Tacrolimus - Teratogenic Agent
• Temtamy preaxial brachydactyly syndrome
• Tetra-Amelia, Autosomal Recessive
• Tetraamelia with pulmonary hypoplasia
• Thomas syndrome
• Thomas Syndrome: Potter Sequence with cleft lip/palate and cardiac anomalies
• Thrombocytopenia - Robin sequence
• Tibial hemimelia - cleft lip/palate
• Tobramycin - Teratogenic Agent
• Tollner-Horst-Manzke syndrome
• Treacher-Collins Syndrome
• Trigonocephaly - bifid nose - acral anomalies
• Triploid syndrome
• Trisomy 13 mosaicism
• Trisomy 14 Mosaic
• Trisomy 14 Mosaicism Syndrome
• Trisomy 18 mosaicism
• Trisomy 18 Syndrome
• Trisomy 3 mosaicism
• Trisomy 6
• Trisomy 8 mosaicism
• Turner-mongolism polysyndrome
• VACTERL with hydrocephalus, X-linked
• Valproic Acid - Teratogenic Agent
• Valsartan - Teratogenic Agent
• Van der Woude syndrome
• Van der Woude syndrome 2
• Varadi Papp syndrome
• Velocardiofacial syndrome
• Velopharyngeal incompetence
• Ventricular extrasystoles perodactyly Robin sequence
• Verloove Vanhorick Brubakk syndrome
• W syndrome
• Waardenburg type pierpont
• Wagner-Stickler Syndrome
• Warman Mulliken Hayward syndrome
• Weaver Johnson syndrome
• Weaver Williams syndrome
• Wildervanck syndrome
• Willems De vries syndrome
• Zadik Barak Levin syndrome
• Zunich neuroectodermal syndrome
• Zunich-Kaye syndrome

About underlying conditions:

With a diagnosis of Cleft palate, it is important to consider whether there is an underlying condition causing Cleft palate. These are other medical conditions that may possibly cause Cleft palate. For general information on this form of misdiagnosis, see Underlying Condition Misdiagnosis or Overview of Misdiagnosis.
 » Next page: Associated Conditions of Cleft palate

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