Preferred Name |
CREST syndrome |
|
Synonyms |
Calcinosis-Raynaud phenomenon-esophageal involvement-sclerodactyly-telangiectasia syndrome |
|
ID |
http://www.orpha.net/ORDO/Orphanet_90290 |
|
alternative_term |
Calcinosis-Raynaud phenomenon-esophageal involvement-sclerodactyly-telangiectasia syndrome |
|
expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90290 |
|
hasDbXref |
ICD-11:4A42.2 ICD-10:M34.1 UMLS:C0206138 MeSH:D017675 MedDRA:10011380 |
|
label |
CREST syndrome |
|
notation |
ORPHA:90290 |
|
prefixIRI |
ORDO:Orphanet_90290 |
|
prefLabel |
CREST syndrome |
|
reason_for_obsolescence |
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Limited cutaneous systemic sclerosis |
|
subClassOf |
Create mapping