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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 77 (DOID:0112168)
Alliance: disease page
Synonyms: DFNA77
Alt IDs: OMIM:618915
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the ABCC1 gene on chromosome 16p13.11.

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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04/09/2024
MGI 6.23 		The Jackson Laboratory