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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photosensitive trichothiodystrophy
MONDO:0002470
xeroderma pigmentosum, autosomal dominant, mild
MONDO:0008690
ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia
MONDO:0008842
Bloom syndrome
MONDO:0008876
COFS syndrome
MONDO:0008926
Nijmegen breakage syndrome
MONDO:0009623