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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 2B (DOID:0110559)
Alliance: disease page
Synonyms: autosomal dominant deafness 2B; DFNA2B
Alt IDs: OMIM:612644, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized postlingual onset in the fourth decade of life with by high frequency progressive hearing loss and has_material_basis_in mutation in the GJB3 gene on chromosome 1p34.3.

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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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last database update
MGI 6.22
The Jackson Laboratory