{"orpha":90290,"name":"CREST syndrome","type":"Clinical subtype","group":"Subtype of disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["Calcinosis-Raynaud phenomenon-esophageal involvement-sclerodactyly-telangiectasia syndrome"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Limited cutaneous systemic sclerosis","url":"https://raremap.alftech.space/d/ORPHA-90290/","orphanet_url":"https://www.orpha.net/en/disease/detail/90290","names":{"fr":{"name":"Syndrome CREST","synonyms":["Syndrome de calcinose-maladie de Raynaud-troubles moteurs oesophagiens-sclérodactylie-télangiectasie"]},"de":{"name":"CREST-Syndrom","synonyms":["Calzinosis - Raynaud Phänomen - ösophageale Dysfunktion - Sklerodaktylie - Telangiektasie"]},"es":{"name":"Síndrome CREST","synonyms":["Calcinosis-fenómeno de Raynaud-afectación esofágica-esclerodactilia-telangiectasia"]},"it":{"name":"Sindrome CREST"},"nl":{"name":"CREST-syndroom","synonyms":["Calcinose - fenomeen van Raynaud - oesofageale betrokkenheid - sclerodactylie - teleangiëctasie-syndroom"]},"pt":{"name":"Síndrome CREST","synonyms":["Síndrome de calcinose-fenómeno de Raynaud-envolvimento esofágico-esclerodactilia-telangiectasia"]},"pl":{"name":"Zespół CREST","synonyms":["Kalcynoza - fenomen Raynauda - zmiany w przełyku - sklerodaktylia - telangiektazja"]},"cs":{"name":"CREST syndrom","synonyms":["Syndrom zahrnující kalcinózu, Raynaudův fenomén, postižení jícnu, sklerodaktylii a teleangiektázii"]},"uk":{"name":"Синдром CREST","synonyms":["Синдром кальцинозу - феномена Рейно - ураження стравоходу - склеродактилії - телеангіектазії"]},"zh":{"name":"CREST综合征","synonyms":["钙化-雷诺现象-食管受累-硬指症-毛细血管扩张综合征"]},"tr":{"name":"CREST sendromu","synonyms":["Kalsinoz-Raynaud fenomeni-Özofageal tutulumu-sklerodaktili-telenjiektazi sendromu"]}},"xrefs":[{"source":"ICD-10","code":"M34.1","qualifier":"E","icd_relation":"specific","validated":true},{"source":"MeSH","code":"D017675","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0206138","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10011380","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":220402,"name":"Limited cutaneous systemic sclerosis"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}