| Descriptor English: | CREST Syndrome | ||||||
| Descriptor Spanish: |
Síndrome CREST
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| Descriptor Portuguese: | Síndrome CREST | ||||||
| Descriptor French: | Syndrome CREST | ||||||
| Entry term(s): |
CREST Syndromes CRST Syndrome CRST Syndromes Calcinosis Raynaud Phenomenon Sclerodactyly Telangiectasia Calcinosis, Raynaud's phenomenon, Esophageal dismobility, Sclerodactyly, Telangiectasia Syndrome Calcinosis-Raynaud Phenomenon-Sclerodactyly-Telangiectasia Phenomenon-Sclerodactyly-Telangiectasia, Calcinosis-Raynaud Syndrome, CREST Syndrome, CRST |
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| Tree number(s): |
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 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D017675 | ||||||
| Scope note: | 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. |
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| Annotation: | CREST syndrome: an acronym for Calcinosis, Raynaud phenomenon, Esophageal dysfunction, Sclerodactyly, Telangiectasis |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Calcinosis (1975-1993) Raynaud's Disease (1975-1993) Scleroderma, Systemic (1975-1993) |
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| Public MeSH Note: | 1994 |
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| History Note: | 1994 |
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| DeCS ID: | 31538 | ||||||
| Unique ID: | D017675 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1994/01/01 | ||||||
| Date of Entry: | 1992/12/28 | ||||||
| Revision Date: | 2012/07/03 |
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CREST Syndrome
- Preferred
CRST Syndrome
- Narrower
| Concept UI |
M0026732 |
| Scope note | 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. |
| Preferred term | CREST Syndrome |
| Entry term(s) |
CREST Syndromes Calcinosis, Raynaud's phenomenon, Esophageal dismobility, Sclerodactyly, Telangiectasia Syndrome Syndrome, CREST |
| Concept UI |
M0026731 |
| Preferred term | CRST Syndrome |
| Entry term(s) |
CRST Syndromes Calcinosis Raynaud Phenomenon Sclerodactyly Telangiectasia Calcinosis-Raynaud Phenomenon-Sclerodactyly-Telangiectasia Phenomenon-Sclerodactyly-Telangiectasia, Calcinosis-Raynaud Syndrome, CRST |
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