Stargardt Disease 1 (STGD1)

Alias:
Fundus Flavimaculatus
Retinal Dystrophy, Early-Onset Severe
Stgd1
Stargardt's Disease
Severe Early-Childhood-Onset Retinal Dystrophy
Early Onset and Severe Retinal Dystrophy
Macular Dystrophy with Flecks, Type 1
Macular Dystrophy with Flecks Type 1
Macular Degeneration, Juvenile
Juvenile Macular Degeneration
Macular Degeneration Juvenile
Stargardt Disease, Type 1
Stgd
Ffm
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Stargardt Disease 1, also known as fundus flavimaculatus, is related to retinoschisis 1, x-linked, juvenile and macular dystrophy, patterned, 1. An important gene associated with Stargardt Disease 1 is ABCA4 (ATP Binding Cassette Subfamily A Member 4), and among its related pathways/superpathways is Ciliopathies. The drugs Vitamin A and Acetic acid have been mentioned in the context of this disorder. Affiliated tissues include retina and eye, and related phenotypes are bull's eye maculopathy and macular degeneration
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
20
163
262

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