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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 58 (DOID:0110582)
Alliance: disease page
Synonyms: autosomal dominant deafness 58; DFNA58
Alt IDs: OMIM:615654, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 2p21-p12.


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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
12/10/2024
MGI 6.24
The Jackson Laboratory