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Summary Literature (0)
DOID:0110586 - autosomal dominant nonsyndromic deafness 65


Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the TBC1D24 gene on chromosome 16p13.

Synonyms: DFNA65, autosomal dominant deafness 65

Xenbase Genes : tbc1d24.1, tbc1d24.2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014470 - autosomal dominant nonsyndromic hearing loss 65


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)