Usher syndrome type 2C

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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 type IIC,

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: adgrv1

OMIM:

MIM:605472 - usher syndrome, type iic; ush2c usher syndrome, type iic, gpr98/pdzd7, digenic, included;; usher syndrome, type iib, formerly, included; ush2b, formerly, included

MIM:605472 - usher syndrome, type iic; ush2c usher syndrome, type iic, gpr98/pdzd7, digenic, included;; usher syndrome, type iib, formerly, included; ush2b, formerly, included

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): Usher syndrome type 2 (is_a)