Xeroderma pigmentosum group C

MONDO:0010211

An autosomal recessive inherited disorder caused by mutations in the XPC gene. This disease is characterized by increased sensitivity to sunlight with the development of carcinomas at an early age and is caused by a defect in nucleotide excision repair.

Also known as: XP-C, XP3, XPC, XPCC, xeroderma pigmentosum group C, xeroderma pigmentosum group type C, xeroderma pigmentosum, complementation group type C, xeroderma pigmentosum, group C

3 clinical trials for this condition and its sub-types, 0 tagged with Xeroderma pigmentosum group C itself.

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↑ Xeroderma pigmentosum (6)

Including sub-types (3) Tagged with Xeroderma pigmentosum group C (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.