Usher Syndrome, Type Ic (USH1C)

Alias:

Usher Syndrome, Type 1c

Usher Syndrome Type 1c

Ush1c

Usher Syndrome Type I Acadian Variety

Usher Syndrome Type Ic

Usher Syndrome, Type I, Acadian Variety

Usher's Syndrome Type 1c

Acadian Usher Syndrome

Usher Syndrome 1c

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Usher Syndrome, Type Ic, also known as usher syndrome, type 1c, is related to deafness, autosomal dominant 65 and usher syndrome, type iic. An important gene associated with Usher Syndrome, Type Ic is USH1C (USH1 Protein Network Component Harmonin), 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：USH039

OMIM：276904

MESH：D052245