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:0110545 - autosomal dominant nonsyndromic deafness 13


Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade of life with mid-frequency hearing loss and has_material_basis_in mutation in the COL11A2 gene on chromosome 6p21.

Synonyms: DFNA13, autosomal dominant deafness 13

Xenbase Genes : col11a2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011159 - autosomal dominant nonsyndromic deafness 13

OMIM:
OMIM:601868 - DEAFNESS, AUTOSOMAL DOMINANT 13; DFNA13

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

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