autosomal dominant nonsyndromic deafness 25

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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,

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

OMIM:

MIM:605583 - deafness, autosomal dominant 25; dfna25

MIM: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)