Scleroderma
MONDO:0019340Scleroderma 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).
Also known as: scleroderma, scleroderma (disease)
339 clinical trials for this condition and its sub-types, 47 tagged with Scleroderma itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Scleroderma
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Systemic sclerosis 261 trials · 295 incl. sub-types
6 sub-types
- Diffuse scleroderma 82 trials
- Diffuse cutaneous systemic sclerosis 30 trials
- Pulmonary systemic sclerosis 27 trials
- Limited cutaneous systemic sclerosis 2 trials Sub-types →
- Limited systemic sclerosis 0 trials
- Scleroderma, familial progressive 0 trials
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Localized scleroderma 14 trials · 15 incl. sub-types
2 sub-types
- Linear scleroderma 1 trial
- Lipodermatosclerosis 1 trial
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Neonatal scleroderma 0 trials