Usher Syndrome, Type Iic (USH2C)

Alias:

Usher Syndrome Type 2c

Usher Syndrome, Type Iic, Gpr98/pdzd7 Digenic

Usher Syndrome, Type 2c

Ush2c

Usher Syndrome Type Iic

Usher Syndrome, Type 2c, Gpr98/pdzd7 Digenic

Usher Syndrome Type Iic Gpr98/pdzd7 Digenic

Usher Syndrome,, Type Iic

Usher's Syndrome Type 2c

Usher Syndrome Iic

Usher Syndrome 2c

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Usher Syndrome, Type Iic, also known as usher syndrome type 2c, is related to retinal degeneration and usher syndrome, type iia. An important gene associated with Usher Syndrome, Type Iic is ADGRV1 (Adhesion G Protein-Coupled Receptor V1), and among its related pathways/superpathways are GPCRs, other and GPCRs, class B secretin-like. Affiliated tissues include retina and eye, and related phenotypes are congenital sensorineural hearing impairment and rod-cone dystrophy

Related ID：

MALACARDS：USH020

OMIM：605472

MESH：D052245