autosomal dominant nonsyndromic deafness 36

Summary

DOID:0110563 - autosomal dominant nonsyndromic deafness 36

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and has_material_basis_in mutation in the TMC1 gene on chromosome 9q21.

Synonyms: autosomal dominant deafness 36, DFNA36

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

: tmc1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011708 - autosomal dominant nonsyndromic hearing loss 36

MONDO:0011708 - autosomal dominant nonsyndromic hearing loss 36

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)