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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 12 (DOID:0110544)
Alliance: disease page
Synonyms: autosomal dominant deafness 8; autosomal dominant deafness 12; DFNA8; DFNA12
Alt IDs: OMIM:601543, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and mid-frequency hearing loss and has_material_basis_in mutation in the TECTA gene on chromosome 11q23.

Disease References using Mouse Models (2)

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 6.13
The Jackson Laboratory