autosomal dominant nonsyndromic deafness

Summary

DOID:0050564 - autosomal dominant nonsyndromic deafness

Disease Ontology Definition:A nonsyndromic deafness characterized by an autosomal dominant inheritance mode.

Synonyms: autosomal dominant deafness

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

: tgfbr1, tjp2, six1, lmx1a, tecta.2, slc44a4, eya4, grhl2, gjb3, kitlg, actg1, myo7a, pou4f3, osbpl2, diaph3, [+]

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0019587 - autosomal dominant nonsyndromic hearing loss

MONDO:0019587 - autosomal dominant nonsyndromic hearing loss

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

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

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