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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 : pou4f3, myo7a, six1
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
nonsyndromic deafness (is_a)