About   Help   FAQ
Disease Ontology Browser
Usher syndrome type 2C (DOID:0110839)
Synonyms: USH2C; 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 (4)
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
08/15/2017
MGI 6.10 		The Jackson Laboratory