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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 79 (DOID:0112160)
Alliance: disease page
Synonyms: DFNA79
Alt IDs: OMIM:619086
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the SCD5 gene on chromosome 4q21.22.

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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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MGI 6.22
The Jackson Laboratory