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Summary Literature (0)
DOID:0110555 - autosomal dominant nonsyndromic deafness 25


Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second-sixth decade of life with high frequency progressive hearing loss and has_material_basis_in mutation in the SLC17A8 gene on chromosome 12q23.

Synonyms: DFNA25, autosomal dominant deafness 25

Xenbase Genes : slc17a8

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011568 - autosomal dominant nonsyndromic deafness 25

OMIM:
OMIM:605583 - DEAFNESS, AUTOSOMAL DOMINANT 25; DFNA25

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)