autosomal dominant nonsyndromic deafness 17

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Summary

Literature (0)

DOID:0110548 - autosomal dominant nonsyndromic deafness 17

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 MYH9 gene on chromosome 22q12.

Synonyms: DFNA17, autosomal dominant deafness 17,

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

OMIM:

MIM:603622 - deafness, autosomal dominant 17; dfna17 cochleosaccular degeneration, included

MIM:603622 - deafness, autosomal dominant 17; dfna17 cochleosaccular degeneration, included

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant nonsyndromic deafness (is_a)