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- B4fcaa0cf2c6c5bd8278f9be19615049f hasDbXref "Orphanet:801" @default.
- B4fcaa0cf2c6c5bd8278f9be19615049f type Axiom @default.
- B4fcaa0cf2c6c5bd8278f9be19615049f annotatedProperty IAO_0000115 @default.
- B4fcaa0cf2c6c5bd8278f9be19615049f annotatedSource MONDO_0019340 @default.
- B4fcaa0cf2c6c5bd8278f9be19615049f annotatedTarget "Scleroderma is a rare autoimmune connective tissue disorder characterized by abnormal hardening of the skin and, sometimes, other organs. It is classified into two main forms: localized scleroderma and systemic sclerosis (SSc), the latter comprising three subsets; diffuse cutaneous SSc (dcSSc), limited cutaneous SSc (lcSSc) and limited SSc (lSSc)." @default.