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: autosomal dominant deafness 23, DFNA23

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

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

: six1

MIM:

MIM:605192 - deafness, autosomal dominant 23; dfna23

MIM:605192 - deafness, autosomal dominant 23; dfna23

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)