Retinitis Pigmentosa 4 (RP4)

Retinitis Pigmentosa 4(来自ICD-11)

别称:

Rp4

Retinitis Pigmentosa 4, Autosomal Dominant or Recessive

Retinitis Pigmentosa, Rhodopsin-Related

Retinitis Pigmentosa, Type 4

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Retinitis Pigmentosa 4, also known as rp4, is related to usher syndrome and retinitis pigmentosa. An important gene associated with Retinitis Pigmentosa 4 is RHO (Rhodopsin), and among its related pathways/superpathways are Visual phototransduction and Visual Cycle in Retinal Rods. Affiliated tissues include retina and eye, and related phenotypes are abnormal electroretinogram and reduced visual acuity

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