CREST Syndrome

**Definition:** 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.

**Tree numbers:** - C06.405.117.119.500.204 - C14.907.355.830.573.750.500 - C14.907.617.812.500 - C14.907.823.225 - C17.300.799.801.500 - C17.800.784.801.500 - C17.800.862.406.750.500 - C18.452.174.130.204

**Synonyms:** - Calcinosis, Raynaud's phenomenon, Esophageal dismobility, Sclerodactyly, Telangiectasia Syndrome