About   Help   FAQ
Disease Ontology Browser
autosomal dominant nonsyndromic deafness 15 (DOID:0110546)
Alliance: disease page
Synonyms: autosomal dominant deafness 15; DFNA15
Alt IDs: OMIM:602459, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the POU4F3 gene on chromosome 5q32.

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