Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0110839 - Usher syndrome type 2C

Disease Ontology Definition:An Usher syndrome type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the ADGRV1 gene on chromosome 5q14.

Synonyms: USH2C, Usher syndrome IIC, Usher syndrome type IIC

Xenbase Genes : adgrv1, pdzd7

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011558 - Usher syndrome type 2C

MIM:
MIM:605472 - USHER SYNDROME, TYPE IIC; USH2C

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): digenic disease (is_a), Usher syndrome type 2 (is_a)