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