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
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
#
Gene
Function
Score
Count
No data available
Drugs
Name
CAS Number
Status
Phase
No data available
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available
References
Title
PMID
Journal
Year
IF
No Data Found!
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Comparison
Al agent
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