About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory