autosomal dominant nonsyndromic deafness 25

Summary

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,

Xenbase 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

: slc17a8

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011568 - autosomal dominant nonsyndromic hearing loss 25

MONDO:0011568 - autosomal dominant nonsyndromic hearing loss 25

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)