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Terminology chevron_right Concepts chevron_right 156453002

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Calcinosis, raynaud's phenomenon, sclerodactyly, oesophageal dysfunction, telangiectasia syndrome
Calcinosis, raynaud's phenomenon, sclerodactyly, esophageal dysfunction, telangiectasia syndrome
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Calcinosis, raynaud's phenomenon, sclerodactyly, oesophageal dysfunction, telangiectasia syndrome

SCTID: 156453002, Primitive, Inactive


156453002|Calcinosis, raynaud's phenomenon, sclerodactyly, oesophageal dysfunction, telangiectasia syndrome|
  • en Calcinosis, raynaud's phenomenon, sclerodactyly, oesophageal dysfunction, telangiectasia syndrome (disorder)
  • en Calcinosis, raynaud's phenomenon, sclerodactyly, esophageal dysfunction, telangiectasia syndrome
  • en Calcinosis, raynaud's phenomenon, sclerodactyly, oesophageal dysfunction, telangiectasia syndrome

156453002 |Calcinosis, raynaud's phenomenon, sclerodactyly, oesophageal dysfunction, telangiectasia syndrome|

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