Log In|Sign Up
ENRetinitis Pigmentosa 41 (RP41)
Alias:
Rp41
Retinal Degeneration, Autosomal Recessive, Prominin-Related
Retinal Degeneration Autosomal Recessive Prominin-Related
Retinitis Pigmentosa, Type 41
Retinitis Pigmentosa-41
Favorite
Retinitis Pigmentosa 41, also known as rp41, is related to malignant astrocytoma and usher syndrome, type ig. An important gene associated with Retinitis Pigmentosa 41 is PROM1 (Prominin 1). Affiliated tissues include retina and eye, and related phenotypes are optic disc pallor and macular degeneration
Related ID：
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
Gene & Mutation
#
Gene
Function
Score
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
References Literature
Title
PMID
Journal
Year
IF
