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Summary Literature (0)
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 : coch

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011058 - autosomal dominant nonsyndromic deafness 9

OMIM:
OMIM:601369 - DEAFNESS, AUTOSOMAL DOMINANT 9; DFNA9

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)