autosomal dominant nonsyndromic deafness 13

Summary

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: autosomal dominant deafness 13, DFNA13

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

: col11a2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011159 - autosomal dominant nonsyndromic hearing loss 13

MONDO:0011159 - autosomal dominant nonsyndromic hearing loss 13

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)