autosomal dominant nonsyndromic deafness 69

Summary

DOID:0110590 - autosomal dominant nonsyndromic deafness 69

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the KITLG gene on chromosome 12q21.

Synonyms: autosomal dominant deafness 69, DCUA, DFNA69, unilateral or asymmetric congenital deafness

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

: kitlg

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014738 - autosomal dominant nonsyndromic hearing loss 69

MONDO:0014738 - autosomal dominant nonsyndromic hearing loss 69

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)