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DOID:0110563 - autosomal dominant nonsyndromic deafness 36
Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and has_material_basis_in mutation in the TMC1 gene on chromosome 9q21.
Synonyms: DFNA36, autosomal dominant deafness 36,
Echinobase Genes :
MIM:606705 - deafness, autosomal dominant 36; dfna36 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee