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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,
Xenbase Genes : tgfbr1, tjp2, six1, lmx1a, tecta.2, slc44a4, eya4, grhl2, gjb3, kitlg, actg1, myo7a, pou4f3, osbpl2, diaph3,
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