Systemic Scleroderma

Alias:
Scleroderma
Progressive Systemic Sclerosis
Systemic Sclerosis
Scleroderma, Familial Progressive
Familial Progressive Scleroderma
Progressive Scleroderma
Scleroderma, Systemic
Scleroderma Syndrome
Diffuse Scleroderma
Scleroderma Disease
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Systemic Scleroderma, also known as scleroderma, is related to scleroderma, familial progressive and limited scleroderma, and has symptoms including exanthema, pruritus and hidebound skin. An important gene associated with Systemic Scleroderma is TSIX (TSIX Transcript, XIST Antisense RNA), and among its related pathways/superpathways are Complement cascade and Senescence and autophagy in cancer. The drugs Ambrisentan and Tadalafil have been mentioned in the context of this disorder. Affiliated tissues include skin and lung, and related phenotypes are homeostasis/metabolism and cardiovascular system
Related ID:
MESH:D012595

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
All ages
1-9/100000
45
537
3

Medical Symptom

#
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
No Data Found!
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