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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 80 (DOID:0070602)
Alliance: disease page
Synonyms: autosomal dominant deafness 80; DFNA80
Alt IDs: OMIM:619274
Definition: An autosomal dominant nonsyndromic deafness characterized by congenital deafness associated with absent or malformed cochleae and eighth cranial nerves that has_material_basis_in heterozygous mutation in the GREB1L gene on chromosome 18q11.

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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Send questions and comments to User Support. 		last database update
10/09/2024
MGI 6.24 		The Jackson Laboratory