autosomal dominant nonsyndromic deafness 3A Disease Ontology Browser

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Disease Ontology Browser

autosomal dominant nonsyndromic deafness 3A (DOID:0110564)
Alliance: disease page
Synonyms: autosomal dominant deafness 3A; DFNA3A
Alt IDs: OMIM:601544, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by prelingual, high frequency hearing loss and has_material_basis_in mutation in the GJB2 gene on chromosome 13q12.

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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