autosomal dominant nonsyndromic deafness 43

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 (0)

DOID:0110568 - autosomal dominant nonsyndromic deafness 43

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 2p12.

Synonyms: DFNA43, autosomal dominant deafness 43,

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

:

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012030 - autosomal dominant nonsyndromic hearing loss 43

MONDO:0012030 - autosomal dominant nonsyndromic hearing loss 43

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

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

Parent(s): autosomal dominant nonsyndromic deafness (is_a)