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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,

Xenbase Genes : six1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011519 - autosomal dominant nonsyndromic hearing loss 23

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant nonsyndromic deafness (is_a)