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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)
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Send questions and comments to User Support. 		last database update
04/23/2024
MGI 6.23 		The Jackson Laboratory