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Ontology Browser

Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis (DOID:9004026)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
anodontia +     
Carvajal syndrome +     
Ackerman Syndrome 
ADULT syndrome  
Aloi Tomasini Isaia Syndrome 
anodontia +   
Anodontia of Permanent Dentition  
anterior segment dysgenesis 4  
AREDYLD Syndrome 
autosomal dominant congenital deafness with onychodystrophy  
Axenfeld-Rieger syndrome type 1  
Axenfeld-Rieger syndrome type 2 
blepharocheilodontic syndrome +   
Book Syndrome 
Carabelli Anomaly of Maxillary Molar Teeth 
Cleft Palate, Deafness, and Oligodontia 
Cleidocranial Dysplasia, Forme Fruste, Dental Anomalies Only  
CODAS syndrome  
Congenital Deafness with Inner Ear Agenesis, Microtia, and Microdontia  
Craniosynostosis and Dental Anomalies  
Deafness Oligodontia Syndrome 
Dens in Dente +  
dental enamel hypoplasia +   
dentin dysplasia +   
dentinogenesis imperfecta +   
Dermatoosteolysis Kirghizian Type 
Diastema +  
Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis  
Dysmyelinating Leukodystrophy with Oligodontia  
Ectodermal Dysplasia, Trichoodontoonychial Type 
Euhidrotic Ectodermal Dysplasia 
Fused Teeth 
Growth Retardation, Alopecia, Pseudoanodontia and Optic Atrophy  
Grubben de Cock Borghgraef Syndrome 
Hypodontia Oligodontia with Orofacial Cleft 
hypohidrotic ectodermal dysplasia +   
hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism  
KBG syndrome  
LADD syndrome  
Larsen syndrome  
Late-Onset Localized Junctional Epidermolysis Bullosa with Mental Retardation 
Lethal Faciocardiomelic Dysplasia 
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Mehta Lewis Patton Syndrome 
Microdontia Hypodontia Short Stature 
Nance-Horan syndrome  
oculodentodigital dysplasia +   
Oculoskeletodental Syndrome  
Odd Shapes of Teeth 
Odontodysplasia +   
Odontomicronychial Dysplasia 
Odontotrichoungual-Digital-Palmar Syndrome 
Oligodontia-Colorectal Cancer Syndrome  
Oroacral Syndrome, Verloes-Koulischer Type 
Otodental Dysplasia 
Pinheiro Freire-Maia Miranda Syndrome 
Postaxial Polydactyly, with Dental and Vertebral Anomalies 
Rodrigues Blindness 
Schopf-Schulz-Passarge syndrome  
solitary median maxillary central incisor  
Split-Hand and Split-Foot With Hypodontia 
Spondyloepimetaphyseal Dysplasia with Abnormal Dentition 
Supernumerary Tooth +   
Taurodontia, Absent Teeth, Sparse Hair 
Taurodontism +  
Taurodontism, Microdontia, and Dens Invaginatus 
Teeth Noneruption of with Maxillary Hypoplasia and Genu Valgum 
temtamy preaxial brachydactyly syndrome  
Thai Symphalangism Syndrome 
Thumb Deformity, Alopecia, Pigmentation Anomaly 
tooth agenesis +   
tooth and nail syndrome  
Tricho-Dento-Osseous Syndrome 1 
Weyers acrofacial dysostosis  
X-Linked Hypodontia 
Zadik Barak Levin Syndrome 
Zazam Sheriff Phillips Syndrome 

Exact Synonyms: DCWHKTA ;   dilated cardiomyopathy with woolly hair, palmoplantar keratoderma, and tooth agenesis
Primary IDs: OMIM:615821
Alternate IDs: RDO:9000791

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.