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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


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

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