SNOMED CT Concept  138875005

Clinical finding  404684003

Finding of limb structure  302293008

Disorder of limb  128605003

Disorder of digit  128597007

CREST syndrome   31848007

SNOMED CT code


SNOMED code31848007
nameCREST syndrome
statusactive
date introduced2002-01-31
fully specified name(s)Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder)
synonyms
  • CREST - Calcinosis, Raynaud's phenomenon, oesophageal dysfunction, sclerodactyly, telangiectasia
  • CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, oesophageal involvement, telangiectasia syndrome
  • CREST - Calcinosis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, telangiectasia
  • CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, esophageal involvement, telangiectasia syndrome
  • Calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome
  • Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome
  • Calcinosis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome
  • Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome
  • Calcinosis, Raynaud phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome
  • Calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia syndrome
  • Calcinosis cutis, Raynaud's, oesophageal dysfunction, sclerodactyly AND telangiectasia
  • CREST syndrome
  • Calcinosis cutis, Raynaud's, esophageal dysfunction, sclerodactyly AND telangiectasia
attributes - group4
Associated morphologyFibrosis   112674009
Finding siteConnective tissue structure   21793004
Pathological processAutoimmune process   263680009
attributes - group3
Finding sitePeripheral vascular system structure   51833009
attributes - group1
Finding siteSkin of digit   279064005
Associated morphologyPathologic calcification   18115005
attributes - group5
Associated morphologyTelangiectasis   112641009
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of limb structure   302293008
      Disorder of limb   128605003
        Disorder of digit   128597007
          CREST syndrome   31848007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Calcinosis   6595006
          Calcinosis cutis   21323007
            CREST syndrome   31848007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Systemic disease   56019007
        Systemic disease affecting skin   238980001
          CREST syndrome   31848007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Systemic disease   56019007
        Systemic sclerosis   89155008
          Limited systemic sclerosis   299276009
            Systemic sclerosis with limited cutaneous involvement   298285004
              CREST syndrome   31848007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Cardiovascular finding   106063007
      Raynaud's phenomenon   266261006
        Secondary Raynaud's phenomenon   356198000
          CREST syndrome   31848007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Cardiovascular finding   106063007
      Disorder of cardiovascular system   49601007
        CREST syndrome   31848007

ancestors
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