Usher Syndrome, Type Iia (USH2A)

Alias:

Usher Syndrome Type 2a

Ush2a

Usher Syndrome, Type 2a

Usher Syndrome Type Iia

Retinal Disease in Usher Syndrome Type Iia, Modifier of

Usher's Syndrome Type 2a

Usher Syndrome,, Type 2a

Usher Syndrome 2a

Ushiia

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Usher Syndrome, Type Iia, also known as usher syndrome type 2a, is related to retinal disease and night blindness. An important gene associated with Usher Syndrome, Type Iia is USH2A (Usherin), and among its related pathways/superpathways are Olfactory Signaling Pathway and Ciliary landscape. Affiliated tissues include retina and eye, and related phenotypes are congenital sensorineural hearing impairment and rod-cone dystrophy

Related ID：

MALACARDS：USH037

OMIM：276901

MESH：D052245