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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 2A (DOID:0110558)
Alliance: disease page
Synonyms: autosomal dominant deafness 2A; DFNA2A
Alt IDs: OMIM:600101, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by high frequency progressive hearing loss and has_material_basis_in mutation in the KCNQ4 gene on chromosome 1p34.2.

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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04/09/2024
MGI 6.23 		The Jackson Laboratory