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Concept information

Cardiovascular Diseases > Vascular Diseases > Peripheral Vascular Diseases > Raynaud Disease > CREST Syndrome
... > Digestive System Diseases > Gastrointestinal Diseases > Esophageal Diseases > Deglutition Disorders > Esophageal Motility Disorders > CREST Syndrome
Stomatognathic Diseases > Pharyngeal Diseases > Deglutition Disorders > Esophageal Motility Disorders > CREST Syndrome
Otorhinolaryngologic Diseases > Pharyngeal Diseases > Deglutition Disorders > Esophageal Motility Disorders > CREST Syndrome
Nutritional and Metabolic Diseases > Metabolic Diseases > Calcium Metabolism Disorders > Calcinosis > CREST Syndrome
Cardiovascular Diseases > Vascular Diseases > Telangiectasis > CREST Syndrome
Skin and Connective Tissue Diseases > Skin Diseases > Scleroderma, Systemic > Scleroderma, Limited > CREST Syndrome
Skin and Connective Tissue Diseases > Connective Tissue Diseases > Scleroderma, Systemic > Scleroderma, Limited > CREST Syndrome

Término preferido

CREST Syndrome  

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Tipo

  • mesh:Descriptor

Definición

  • 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.

Concepto genérico

Etiquetas alternativas

  • Calcinosis, Raynaud's phenomenon, Esophageal dismobility, Sclerodactyly, Telangiectasia Syndrome

En otras lenguas

  • Syndrome CREST

    francés

  • Calcinose sous-cutanée, syndrome de Raynaud, dysfonction de l'oesophage, sclérodactylie, télangiectasies

URI

http://data.loterre.fr/ark:/67375/JVR-ZH8TXGWG-L

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RDF/XML TURTLE JSON-LD Creado 28/12/92, última modificación 3/7/12