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Summary Literature (3)
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 : 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

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): nonsyndromic deafness (is_a)