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Ontology Browser

Ichthyosiform Erythroderma, Corneal Involvement, Deafness (DOID:9007169)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Aniridia 1  
autosomal dominant keratitis-ichthyosis-deafness syndrome  
band keratopathy 
Bietti crystalline corneoretinal dystrophy  
Brachymesomelia Renal Syndrome 
Congenital Corneal Opacities, Cornea Guttata, and Corectopia 
Congenital Hereditary Endothelial Dystrophy with Nail Hypoplasia 
Corneal Cerebellar Syndrome 
corneal dystrophy-perceptive deafness syndrome  
corneal endothelial dystrophy +   
Corneodermatoosseous Syndrome 
Dermochondrocorneal Dystrophy of Fran├žois 
EDICT Syndrome  
epithelial and subepithelial dystrophy +   
epithelial-stromal TGFBI dystrophy +   
Ichthyosiform Erythroderma, Corneal Involvement, Deafness  
Judge Misch Wright Syndrome 
Kuster Majewski Hammerstein Syndrome 
Macular Dystrophy, Fenestrated Sheen Type 
Macular Dystrophy, Retinal, 2  
Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus  
Mousa Al din Al Nassar Syndrome 
O'Donnell Pappas Syndrome  
Oculodental Syndrome Rutherfurd Syndrome 
posterior polymorphous corneal dystrophy +   
Progressive Bifocal Chorioretinal Atrophy  
Pseudoinflammatory Fundus Dystrophy, Finnish Type  
Reis-Bucklers corneal dystrophy  
Retinal Macular Dystrophy 1, North Carolina Type  
Ribbonlike Corneal Degeneration with Deafness 
Sammartino De Crecchio Syndrome 
spondyloepiphyseal dysplasia with punctate corneal dystrophy 
spondylometaphyseal dysplasia with corneal dystrophy  
stromal dystrophy +   
Sveinsson chorioretinal atrophy  

Exact Synonyms: Desmons syndrome ;   Ichthyosiform erythroderma, corneal involvement, and deafness ;   Keratitis-ichthyosis-deafness syndrome, autosomal recessive ;   Kid syndrome, autosomal recessive
Primary IDs: MESH:C537363
Alternate IDs: OMIM:242150

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