autosomal dominant nonsyndromic deafness 17

Summary

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: autosomal dominant deafness 17, DFNA17

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

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

: myh9

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011350 - autosomal dominant nonsyndromic hearing loss 17

MONDO:0011350 - autosomal dominant nonsyndromic hearing loss 17

MIM:

MIM:603622 - DEAFNESS, AUTOSOMAL DOMINANT 17; DFNA17

MIM:603622 - DEAFNESS, AUTOSOMAL DOMINANT 17; DFNA17

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

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

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