Cone-Rod Dystrophy 7 (CORD7)

Alias:
Cord7
Dystrophy, Cone-Rod, Type 7
Retinitis Pigmentosa 7
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cone-Rod Dystrophy 7, also known as cord7, is related to fundus dystrophy and retinitis pigmentosa. An important gene associated with Cone-Rod Dystrophy 7 is RIMS1 (Regulating Synaptic Membrane Exocytosis 1), and among its related pathways/superpathways is Synaptic vesicle pathway. Affiliated tissues include eye, and related phenotypes are visual impairment and color vision defect
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
--
9
59
3

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