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Syndrome

CREST Syndrome

AMW:DIS:060053

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.

Pathology clinical
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Graph assertions

CREST Syndrome has parent Calcinosis
CREST Syndrome has parent Esophageal Motility Disorders
CREST Syndrome has parent Raynaud Disease
CREST Syndrome has parent Scleroderma, Limited
CREST Syndrome has parent Telangiectasis

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