Related MeSH Hierarchy (8)
Diseases [C] » Cardiovascular Diseases [C14] » Vascular Diseases » Embolism and Thrombosis » Thrombosis » Livedoid Vasculopathy » Raynaud Disease » CREST Syndrome
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Vascular » Livedoid Vasculopathy » Raynaud Disease » CREST Syndrome
Diseases [C] » Digestive System Diseases [C06] » Gastrointestinal Diseases » Esophageal Diseases » Deglutition Disorders » Esophageal Motility Disorders » CREST Syndrome
Diseases [C] » Cardiovascular Diseases [C14] » Vascular Diseases » Peripheral Vascular Diseases » Raynaud Disease » CREST Syndrome
Diseases [C] » Cardiovascular Diseases [C14] » Vascular Diseases » Telangiectasis » CREST Syndrome
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Connective Tissue Diseases » Scleroderma, Systemic » Scleroderma, Limited » CREST Syndrome
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Scleroderma, Systemic » Scleroderma, Limited » CREST Syndrome
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Calcium Metabolism Disorders » Calcinosis » CREST Syndrome
Description
A mild form of LIMITED SCLERODERMA, a multi-system disorder. Its features include symptoms of CALCINOSIS; RAYNAUD DISEASE; ESOPHAGEAL MOTILITY DISORDERS; sclerodactyly, and TELANGIECTASIS. When the defect in esophageal function is not prominent, it is known as CRST syndrome. MeSH
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Organization Involved with Phase 4 Indications (1)
Organization Involved with Phase 3 Indications (1)
Organization Involved with Phase 1 Indications (1)
Organization Involved with Other Experimental Indications (1)
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UMLS Data
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