Autosomal Recessive Congenital Stationary Night Blindness

Alias:
Night Blindness, Congenital Stationary, Incomplete, Autosomal Recessive
Autosomal Recessive Incomplete Congenital Stationary Night Blindness
Autosomal Recessive Complete Congenital Stationary Night Blindness
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Autosomal Recessive Congenital Stationary Night Blindness, also known as night blindness, congenital stationary, incomplete, autosomal recessive, is related to cone-rod synaptic disorder, congenital nonprogressive and congenital stationary night blindness. An important gene associated with Autosomal Recessive Congenital Stationary Night Blindness is CABP4 (Calcium Binding Protein 4). Affiliated tissues include retina and eye.
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Unknown
--
1
6
8

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
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
No Data Found!
Wechat
Comparison
Al agent
Tutorials
Back to top