autosomal dominant nonsyndromic deafness 9

Summary

DOID:0110593 - autosomal dominant nonsyndromic deafness 9

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade with high frequency progressive hearing loss and has_material_basis_in mutation in the COCH gene on chromosome 14q12.

Synonyms: DFNA9, autosomal dominant deafness 9,

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

: coch

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011058 - autosomal dominant nonsyndromic hearing loss 9

MONDO:0011058 - autosomal dominant nonsyndromic hearing loss 9

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)