autosomal dominant nonsyndromic deafness 22

Summary

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: autosomal dominant deafness 22, DFNA22

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

: myo6

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011660 - autosomal dominant nonsyndromic hearing loss 22

MONDO:0011660 - autosomal dominant nonsyndromic hearing loss 22

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)