Colorblindness, Partial, Protan Series (CBP)

Alias:
Red Color Blindness
Protan Defect
Protanopia
Colorblindness, Protan
Red Colorblindness
Cbp
Color Blindness, Red
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Colorblindness, Partial, Protan Series, also known as red color blindness, is related to bornholm eye disease and myopia, and has symptoms including visual disturbance An important gene associated with Colorblindness, Partial, Protan Series is OPN1LW (Opsin 1, Long Wave Sensitive), and among its related pathways/superpathways are Visual Cycle in Retinal Rods and Diseases of the neuronal system. Affiliated tissues include retina and eye, and related phenotypes are protanomaly and vision/eye
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XLD
XL
XLR
Unknown
--
12
67
21

Medical Symptom

#
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

Name
CAS Number
Status
Phase
No data available

Disease Model

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

References Literature

Title
PMID
Journal
Year
IF
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