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Disease Ontology Browser
autosomal dominant auditory neuropathy 1 (DOID:0060690)
Alliance: disease page
Synonyms: AUNA1; nonsyndromic dominant auditory neuropathy; NSDAN
Alt IDs: OMIM:609129, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness characterized by preservation of outer hair cell function and abnormal or absent auditory brainstem responses that has_material_basis_in heterozygous mutation in the DIAPH3 gene on chromosome 13q.

Disease References using Mouse Models (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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last database update
MGI 6.22
The Jackson Laboratory