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DOID:0110571 - autosomal dominant nonsyndromic deafness 48
Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with progressive hearing loss and has_material_basis_in variation in the chromosome region 12q13-q14.
Synonyms: DFNA48, autosomal dominant deafness 48,
Echinobase Genes :
MIM:607841 - deafness, autosomal dominant 48; dfna48 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee