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 51 (DOID:0110577)
Alliance: disease page
Synonyms: autosomal dominant deafness 51; chromosome 9q21.11 duplication syndrome; DFNA51
Alt IDs: OMIM:613558, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the fourth decade of life with high frequency progressive hearing loss and has_material_basis_in a 269-kb duplication of chromosome 9q21.11 involving the TJP2 and FAM189A2 genes.

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
MGI 6.22
The Jackson Laboratory