Congenital Stationary Night Blindness

Alias:
Night Blindness, Congenital Stationary
Congenital Essential Nyctalopia
Oguchi Disease
Blindness, Night, Stationary, Congenital
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Congenital Stationary Night Blindness, also known as night blindness, congenital stationary, is related to night blindness, congenital stationary, type 1a and night blindness, congenital stationary, type 1b. An important gene associated with Congenital Stationary Night Blindness is NYX (Nyctalopin), and among its related pathways/superpathways are Olfactory Signaling Pathway and CREB Pathway. The drugs Beta carotene and Carotenoids have been mentioned in the context of this disorder. Affiliated tissues include eye and retina, and related phenotypes are myopia and reduced visual acuity
Related ID:
MESH:C537743

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XLD
AD
AR
XL
Newborn
--
120
843
11

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

Name
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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