Reynolds Syndrome (REYNS)

Alias:
Primary Biliary Cirrhosis and Systemic Scleroderma
Primary Biliary Cirrhosis, Scleroderma, Raynaud Disease, and Telangiectasia
Primary Biliary Cirrhosis Scleroderma Raynaud Disease and Telangiectasia
Reyns
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Reynolds Syndrome, also known as primary biliary cirrhosis and systemic scleroderma, is related to scleroderma, familial progressive and primary biliary cholangitis, and has symptoms including icterus and pruritus. An important gene associated with Reynolds Syndrome is LBR (Lamin B Receptor), and among its related pathways/superpathways are Cell Cycle, Mitotic and Separation of Sister Chromatids. Affiliated tissues include liver and skin, and related phenotypes are hepatomegaly and generalized abnormality of skin
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Adult
--
8
103
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