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Summary Literature (0)
DOID:0110553 - autosomal dominant nonsyndromic deafness 23


Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the SIX1 gene on chromosome 14q23.

Synonyms: DFNA23; autosomal dominant deafness 23

Referenced OMIM:
OMIM:605192 - DEAFNESS, AUTOSOMAL DOMINANT 23; DFNA23

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : six1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant nonsyndromic deafness (is_a)


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