autosomal dominant nonsyndromic deafness 20

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Summary

Literature (0)

DOID:0110550 - autosomal dominant nonsyndromic deafness 20

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the ACTG1 gene on chromosome 17q25.

Synonyms: DFNA20, DFNA26, autosomal dominant deafness 20,

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

OMIM:

MIM:604717 - deafness, autosomal dominant 20; dfna20

MIM:604717 - deafness, autosomal dominant 20; dfna20

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)