Retinitis Pigmentosa (RP)
Alias:
Rod-Cone Dystrophy
Pigmentary Retinopathy
Rp
Pericentral Pigmentary Retinopathy
Non-Syndromic Retinitis Pigmentosa
Tapetoretinal Degeneration
Retinitis Pigmentosa 1
Rcd
Basic Information
Medical Symptom
Gene & Mutation
Drugs
Disease Model
References
Retinitis Pigmentosa, also known as rod-cone dystrophy, is related to cone-rod dystrophy 2 and usher syndrome. An important gene associated with Retinitis Pigmentosa is CRX (Cone-Rod Homeobox), and among its related pathways/superpathways are Olfactory Signaling Pathway and Visual phototransduction. The drugs Vitamin A and Lutein have been mentioned in the context of this disorder. Affiliated tissues include Eye and retina, and related phenotypes are intellectual disability and nystagmus
Related ID:
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Models
Reference
MALACARDS
Mit
AD
XL
XLD
AR
XLR
Child
1-5/10000
128
899
536
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
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Gene
Function
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No data available
Drugs
Name
CAS Number
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Phase
No data available
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available
References
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PMID
Journal
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IF
No Data Found!
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Comparison
Al agent
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