autosomal dominant nonsyndromic deafness 40 Disease Ontology Browser

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Disease Ontology Browser

autosomal dominant nonsyndromic deafness 40 (DOID:0110566)
Alliance: disease page
Synonyms: autosomal dominant deafness 40; DFNA40
Alt IDs: OMIM:616357, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CRYM gene on chromosome 16p12.

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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