Limited Scleroderma

Alias:
Limited Cutaneous Systemic Sclerosis
Systemic Sclerosis Sine Scleroderma
Limited Systemic Sclerosis
Limited Cutaneous Systemic Scleroderma
Scleroderma, Limited
Crest - [calcinosis, Raynaud Phenomenon, Oesophageal Dysmotility, Sclerodactyly, and Telangiectasia] Syndrome
Crst - [calcinosis, Raynaud Phenomenon, Sclerodactyly and Telangiectasia] Syndrome
Systemic Sclerosis, Limited
Crest Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Limited Scleroderma, also known as limited cutaneous systemic sclerosis, is related to systemic scleroderma and scleroderma, familial progressive. An important gene associated with Limited Scleroderma is IRF5 (Interferon Regulatory Factor 5), and among its related pathways/superpathways is Genes associated with the development of rheumatoid arthritis. The drugs Ropivacaine and Sodium citrate have been mentioned in the context of this disorder. Affiliated tissues include skin and bone, and related phenotypes are autoimmunity and hypopigmented skin patches
Related ID:
MESH:D045745
ICD11:187455179

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Adult
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49
446
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Medical Symptom

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Description
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Gene & Mutation

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No data available

Disease Model

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MGI
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Publications
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References Literature

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