autosomal dominant nonsyndromic deafness 11

Summary

DOID:0110543 - autosomal dominant nonsyndromic deafness 11

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the first decade of life with a flat or gently downsloping audioprofiles and has_material_basis_in mutation in the MYO7A gene on chromosome 11q13.

Synonyms: autosomal dominant deafness 11, DFNA11

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

: myo7a

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011032 - autosomal dominant nonsyndromic hearing loss 11

MONDO:0011032 - autosomal dominant nonsyndromic hearing loss 11

MIM:

MIM:601317 - DEAFNESS, AUTOSOMAL DOMINANT 11; DFNA11

MIM:601317 - DEAFNESS, AUTOSOMAL DOMINANT 11; DFNA11

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)