Retinitis Pigmentosa 4 (RP4)

Alias:
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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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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10
66
92

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
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IF
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