ORPHA:90290

CREST syndrome

Synonyms: Calcinosis-Raynaud phenomenon-esophageal involvement-sclerodactyly-telangiectasia syndrome

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Limited cutaneous systemic sclerosis

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	CREST syndrome	Calcinosis-Raynaud phenomenon-esophageal involvement-sclerodactyly-telangiectasia syndrome
fr	Syndrome CREST	Syndrome de calcinose-maladie de Raynaud-troubles moteurs oesophagiens-sclérodactylie-télangiectasie
de	CREST-Syndrom	Calzinosis - Raynaud Phänomen - ösophageale Dysfunktion - Sklerodaktylie - Telangiektasie
es	Síndrome CREST	Calcinosis-fenómeno de Raynaud-afectación esofágica-esclerodactilia-telangiectasia
it	Sindrome CREST
nl	CREST-syndroom	Calcinose - fenomeen van Raynaud - oesofageale betrokkenheid - sclerodactylie - teleangiëctasie-syndroom
pt	Síndrome CREST	Síndrome de calcinose-fenómeno de Raynaud-envolvimento esofágico-esclerodactilia-telangiectasia
pl	Zespół CREST	Kalcynoza - fenomen Raynauda - zmiany w przełyku - sklerodaktylia - telangiektazja
cs	CREST syndrom	Syndrom zahrnující kalcinózu, Raynaudův fenomén, postižení jícnu, sklerodaktylii a teleangiektázii
uk	Синдром CREST	Синдром кальцинозу - феномена Рейно - ураження стравоходу - склеродактилії - телеангіектазії
zh	CREST综合征	钙化-雷诺现象-食管受累-硬指症-毛细血管扩张综合征
tr	CREST sendromu	Kalsinoz-Raynaud fenomeni-Özofageal tutulumu-sklerodaktili-telenjiektazi sendromu

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-10	M34.1	E	specific	validated
MeSH	D017675	E		validated
UMLS	C0206138	E		validated
MedDRA	10011380	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Not placed in any Orphanet classification in this release.

No children.

0 direct

Orphanet records no gene directly on this code.

0 records

No prevalence record in this release.

Orphanet has no HPO annotation for this code in this release.