CR(E)ST syndrome

Preferred Label : CR(E)ST syndrome;

Inclusion CIM-10 : Combination of calcinosis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, telangiectasia;

Diag associé à un acte (%) : 89.3;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

M341;

UMLS CUI

C0206138;

Currated CISMeF NLP mapping
- CR(E)ST syndrome [ICD-10 Sub-category (who)]
- CREST syndrome [DO Concept]
DO Cross reference
- CREST syndrome [DO Concept]
Orphanet concepts
- CREST syndrome [ORDO Disease]
- Limited cutaneous systemic sclerosis [ORDO Disease]
- Systemic sclerosis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- CREST Syndrome [NCIt concept]
- CREST syndrome [MedDRA Preferred Term]
- CREST syndrome [MeSH Descriptor]
- CREST syndrome [MeSH concept]
- CREST syndrome [ORDO Disease]
- CREST syndrome [PASCAL descriptor]
- CREST syndrome [DO Concept]
- Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) [SNOMED CT concept]
- crest syndrome [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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