Night Blindness, Congenital Stationary, Type 1g (CSNB1G)

Alias:
Congenital Stationary Night Blindness 1g
Csnb1g
Blindness, Night, Stationary, Congenital, Type 1g
Congenital Stationary Night Blindness Type 1g
Night Blindness, Congenital Stationary, 1g
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Night Blindness, Congenital Stationary, Type 1g, is also known as congenital stationary night blindness 1g. An important gene associated with Night Blindness, Congenital Stationary, Type 1g is GNAT1 (G Protein Subunit Alpha Transducin 1). Affiliated tissues include bone, and related phenotypes are rod-cone dystrophy and optic disc pallor
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
7
2

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

Title
PMID
Journal
Year
IF
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