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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.

Synonyms:


In Mondo Disease Ontology:
MONDO:0019588 - autosomal recessive nonsyndromic deafness

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : met, tecta.2, esrrb, gjb3, ror1, triobp, myo15a, myo7a, foxi1, tmie, ptprq, kars1, nars2, bsnd, gpsm2, [+]

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): nonsyndromic deafness (is_a)