autosomal dominant nonsyndromic deafness 23

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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,

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: six1

OMIM:

MIM:605192 - deafness, autosomal dominant 23; dfna23

MIM:605192 - deafness, autosomal dominant 23; dfna23

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)