autosomal dominant nonsyndromic deafness 37 Disease Ontology Browser

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Disease Ontology Browser

autosomal dominant nonsyndromic deafness 37 (DOID:0070601)
Alliance: disease page
Synonyms: autosomal dominant deafness 37; DFNA37
Alt IDs: OMIM:618533
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the COL11A1 gene on chromosome 1p21.1.

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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