CREST syndrome

Preferred Label : CREST syndrome;

MeSH 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.;

MeSH synonym : syndrome, crest; calcinosis, raynaud's phenomenon, esophageal dismobility, sclerodactyly, telangiectasia syndrome; CREST syndromes;

CISMeF synonym : CREST;

MeSH hyponym : CRST syndrome; CRST Syndromes; Syndrome, CRST; Calcinosis-Raynaud Phenomenon-Sclerodactyly-Telangiectasia; Calcinosis Raynaud Phenomenon Sclerodactyly Telangiectasia; Phenomenon-Sclerodactyly-Telangiectasia, Calcinosis-Raynaud;

MeSH annotation : CREST syndrome: an acronym for Calcinosis, Raynaud phenomenon, Esophageal dysfunction, Sclerodactyly, Telangiectasis;

Wikipedia link : https://en.wikipedia.org/wiki/Crest syndrome;

Details

Origin ID

D017675;

UMLS CUI

C0206138;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- CRST syndrome [MedDRA LLT]
- Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia syndrome (disorder) [SNOMED CT concept]
- Crest [FMA entity]
- Crest [NCIt concept]
- SS18L1 wt Allele [NCIt concept]
- Scleroderma, familial progressive [OMIM Phenotype]
- Ss18l1 subunit of baf chromatin remodeling complex [OMIM gene]
- Systemic sclerosis (disorder) [SNOMED CT concept]
- Thibierge-Weissenbach syndrome [ICD-11 More detail]
- crest [UBERON concept]
- crst syndrome [SNOMED Notion]
Currated CISMeF NLP mapping
- CR(E)ST syndrome [ICD-10 Sub-category (who)]
- CREST Syndrome [NCIt concept]
- CREST syndrome [PASCAL descriptor]
- CREST syndrome [DO Concept]
- CREST syndrome [MedDRA Preferred Term]
- CREST syndrome [ORDO Disease]
- Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) [SNOMED CT concept]
- Limited systemic sclerosis [ICD-11 Subcategory]
- crest syndrome [SNOMED Notion]
- limited scleroderma [Disease (Nov.)]
DO Cross reference
- CREST syndrome [DO Concept]
Indexing information
- anticentromere antibody [MeSH Supplementary Concept]
Manual NTBT mappings (CISMeF)
- Systemic inflammatory disease associated with an acquired peripheral neuropathy [ORDO Disease]
ORDO relation(s)
- CREST syndrome [ORDO Disease]
Record concept(s)
- CREST syndrome [MeSH concept]
- CRST syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- CR(E)ST syndrome [ICD-10 Sub-category]
- CREST Syndrome [NCIt concept]
- CREST syndrome [ORDO Disease]
- CREST syndrome [MedDRA Preferred Term]
- CREST syndrome [DO Concept]
- CREST syndrome [PASCAL descriptor]
- Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) [SNOMED CT concept]
- crest syndrome [SNOMED Notion]

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