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Summary Literature (6)
DOID:0050565 - autosomal recessive nonsyndromic deafness

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


Xenbase Genes : met, tecta.2, esrrb, gjb3, ror1, triobp, myo15a, myo7a, foxi1, col11a2, tmie, ptprq, kars1, nars2, bsnd, [+]

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019588 - hearing loss, autosomal recessive

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

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