About   Help   FAQ
Disease Ontology Browser
autosomal recessive nonsyndromic deafness (DOID:0050565)
Alliance: disease page
Alt IDs: OMIM:607197, ICD10CM:H90.3, OMIM:PS220290, ORDO:90636
Definition: A nonsyndromic deafness characterized by an autosomal recessive inheritance mode.

Disease References using Mouse Models (50)

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, Copyright, and Privacy Statement
Send questions and comments to User Support.
last database update
MGI 6.22
The Jackson Laboratory