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UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
C C- C1 C3 C5 C6 C7 CA CB CC CD CE CF CG CH CI CJ CK CL CM CN CO CP CQ CR CS CT CU CV CW CX CY CZ
CR3 CRA CRB CRC CRE CRI CRK CRL CRM CRO CRP CRR CRU CRY

CREST syndrome

[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. ( MSH )]
UMLS (CSP) C0206138
 
Disease or Syndrome
Relation/PAR: Calcinosis
DYSKINESIA OF ESOPHAGUS
Raynaud's disease
progressive systemic sclerosis
telangiectasia

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