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Disease Ontology Browser
Usher syndrome type 2C (DOID:0110839)
Alliance: disease page
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
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Send questions and comments to User Support. 		last database update
04/03/2018
MGI 6.11 		The Jackson Laboratory