About   Help   FAQ
On Friday, September 29 at 7:30AM ET, access to MGI will be intermittent for a short time due to maintenance.
Disease Ontology Browser
autosomal dominant nonsyndromic deafness 56 (DOID:0110581)
Alliance: disease page
Synonyms: autosomal dominant deafness 56; DFNA56
Alt IDs: OMIM:615629, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the TNC gene on chromosome 9q33.


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
09/19/2023
MGI 6.22
The Jackson Laboratory