autosomal recessive nonsyndromic deafness

Summary

DOID:0050565 - autosomal recessive nonsyndromic deafness

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

Synonyms:

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: 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

MONDO:0019588 - hearing loss, autosomal recessive

MIM:

MIM:607197 - DEAFNESS, AUTOSOMAL RECESSIVE

MIM:607197 - DEAFNESS, AUTOSOMAL RECESSIVE

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view

Parent(s): autosomal recessive disease (is_a), nonsyndromic deafness (is_a)