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Up to: DNA repair disease · Hereditary photodermatosis
Xeroderma pigmentosum
Xeroderma pigmentosum (XP) is a rare genodermatosis characterized by extreme sensitivity to ultraviolet (UV)-induced changes in the skin and eyes, and multiple skin cancers. It is subdivided into 8 complementation groups, according to the affected gene: classical XP (XPA to XPG) and XP variant (XPV).
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Xeroderma pigmentosum group F 1 trial
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Xeroderma pigmentosum group A 0 trials
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Xeroderma pigmentosum group B 0 trials
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Xeroderma pigmentosum group C 0 trials
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Xeroderma pigmentosum group D 0 trials
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Xeroderma pigmentosum group E 0 trials
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Xeroderma pigmentosum group G 0 trials