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DOID:0110552 - autosomal dominant nonsyndromic deafness 22
Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14.
Synonyms: DFNA22, autosomal dominant deafness 22,
Echinobase Genes :
MIM:606346 - deafness, autosomal dominant 22; dfna22 deafness, autosomal dominant 22, with hypertrophic cardiomyopathy, included |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee