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Summary Literature (0)
DOID:0110544 - autosomal dominant nonsyndromic deafness 12


Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and mid-frequency hearing loss and has_material_basis_in mutation in the TECTA gene on chromosome 11q23.

Synonyms: DFNA12, DFNA8, autosomal dominant deafness 12, autosomal dominant deafness 8

Xenbase Genes : tecta.2, tecta.1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011102 - autosomal dominant nonsyndromic deafness 12

OMIM:
OMIM:601543 - DEAFNESS, AUTOSOMAL DOMINANT 12; DFNA12

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)