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DOID:0110564 - autosomal dominant nonsyndromic deafness 3A
Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by prelingual, high frequency hearing loss and has_material_basis_in mutation in the GJB2 gene on chromosome 13q12.
Synonyms: DFNA3A, autosomal dominant deafness 3A,
Echinobase Genes :
MIM:601544 - deafness, autosomal dominant 3a; dfna3a |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee