About   Help   FAQ
Disease Ontology Browser
autosomal dominant nonsyndromic deafness 11 (DOID:0110543)
Alliance: disease page
Synonyms: autosomal dominant deafness 11; DFNA11
Alt IDs: OMIM:601317, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the first decade of life with a flat or gently downsloping audioprofiles and has_material_basis_in mutation in the MYO7A gene on chromosome 11q13.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.12
The Jackson Laboratory