Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (6)
DOID:0050565 - autosomal recessive nonsyndromic deafness


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

Synonyms:

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

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019588 - autosomal recessive nonsyndromic deafness


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

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