Medical Subject Headings / 医学主题词表

Last uploaded: September 7, 2023
Preferred Name

CREST Syndrome

Synonyms

Syndrome, CREST

Definitions

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.

ID

http://purl.bioontology.org/ontology/MESH/D017675

altLabel

Syndrome, CREST

Calcinosis Raynaud Phenomenon Sclerodactyly Telangiectasia

CRST Syndrome

Calcinosis-Raynaud Phenomenon-Sclerodactyly-Telangiectasia

Syndrome, CRST

Phenomenon-Sclerodactyly-Telangiectasia, Calcinosis-Raynaud

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

CREST Syndromes

CRST Syndromes

AN

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

AQL

BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI

cui

C1527226

C0206138

DC

1

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.

DX

19940101

HN

1994

Inverse of AQ

http://purl.bioontology.org/ontology/MESH/Q000401

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000235

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000151

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000469

Machine permutation

1994

MDA

19921228

MMR

20211018

MN

C06.405.117.119.500.204

C14.907.617.812.500

C18.452.174.130.204

C14.907.823.225

C14.907.355.830.573.750.500

C17.300.799.801.500

C17.800.862.406.750.500

C17.800.784.801.500

notation

D017675

prefLabel

CREST Syndrome

TERMUI

T751302

T052879

T751301

T052878

TH

NLM (1994)

NLM (2010)

ORD (2010)

OMIM (2013)

tui

T047

subClassOf

http://purl.bioontology.org/ontology/MESH/D002114

http://purl.bioontology.org/ontology/MESH/D011928

http://purl.bioontology.org/ontology/MESH/D013684

http://purl.bioontology.org/ontology/MESH/D045745

http://purl.bioontology.org/ontology/MESH/D015154

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http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C70646 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://www.orpha.net/ORDO/Orphanet_90290 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://purl.bmicc.cn/ontology/ICD10CN/M34.1 《国际疾病分类》第10版中文版 / International Classification of Diseases, 10th Edition, China CUI
http://purl.obolibrary.org/obo/DOID_0060218 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.bioontology.org/ontology/ICD10/M34.1 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 CUI
http://purl.bioontology.org/ontology/ICD10/M34.1 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 LOOM
http://purl.obolibrary.org/obo/MONDO_0019563 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.bioontology.org/ontology/ICD10CM/M34.1 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 CUI
http://purl.bioontology.org/ontology/ICD10CM/M34.1 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 LOOM
http://purl.bioontology.org/ontology/OMIM/181750 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI