autosomal dominant nonsyndromic deafness 20 Disease Ontology Browser

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Disease Ontology Browser

autosomal dominant nonsyndromic deafness 20 (DOID:0110550)
Alliance: disease page
Synonyms: autosomal dominant deafness 20; DFNA20; DFNA26
Alt IDs: OMIM:604717, ICD10CM:H90.3
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.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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