Usher Syndrome, Type Id (USH1D)

Alias:

Usher Syndrome, Type 1d

Usher Syndrome Type 1d

Ush1d

Usher Syndrome, Type Id/f, Digenic

Usher Syndrome Type Id

Usher Syndrome, Type 1d/f Digenic

Usher Syndrome, Type 1d/f

Usher's Syndrome Type 1d

Usher's Syndrome Type 1h

Usher Syndrome Type Ih

Usher Syndrome 1d/f

Usher Syndrome 1d

Usher Syndrome 1h

Ush1d/f

Ush1df

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Usher Syndrome, Type Id, also known as usher syndrome, type 1d, is related to retinal degeneration and usher syndrome, type ic. An important gene associated with Usher Syndrome, Type Id is CDH23 (Cadherin Related 23), and among its related pathways/superpathways are Olfactory Signaling Pathway and Sensory processing of sound. Affiliated tissues include retina and eye, and related phenotypes are hearing impairment and rod-cone dystrophy

Related ID：

MALACARDS：USH040

OMIM：601067

MESH：D052245