About   Help   FAQ
Disease Ontology Browser
autosomal recessive nonsyndromic deafness 1A (DOID:0110475)
Synonyms: autosomal recessive deafness 1A; DFNB1A
Alt IDs: OMIM:220290, ICD10CM:H90.3, ORDO:90636
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and has_material_basis_in mutation in the GJB2 gene on chromosome 13q12.

Disease References using Mouse Models (5)

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
04/11/2017
MGI 6.08
The Jackson Laboratory