Xeroderma pigmentosum group G

Any xeroderma pigmentosum in which the cause of the disease is a mutation in the ERCC5 gene.

Also known as: ERCC5 xeroderma pigmentosum, XP-G, XP7, XPG, xeroderma pigmentosum caused by mutation in ERCC5, xeroderma pigmentosum group G, xeroderma pigmentosum group type G, xeroderma pigmentosum, complementation group type G

42 clinical trials for this condition and its sub-types.