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DOID:0050565 - autosomal recessive nonsyndromic deafness
Disease Ontology Definition:A nonsyndromic deafness characterized by an autosomal recessive inheritance mode.
Synonyms:
Echinobase Genes : pcdh15, tbc1d24, myo7a, otof, kars1, whrn, pnpt1, msrb3
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee