About   Help   FAQ
Disease Ontology Browser
Usher syndrome type 2C (DOID:0110839)
Alliance: disease page
Synonyms: USH2C; Usher syndrome IIC; Usher syndrome type IIC
Alt IDs: OMIM:605472, ICD10CM:H35.5
Definition: An Usher syndrome type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the ADGRV1 gene on chromosome 5q14.

Disease References using Mouse Models (5)
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
11/12/2024
MGI 6.24 		The Jackson Laboratory