autosomal dominant nonsyndromic deafness

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Summary

Literature (0)

DOID:0050564 - autosomal dominant nonsyndromic deafness

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

Synonyms: autosomal dominant deafness,

Echinobase 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

: pou4f3, myo7a, six1

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)