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Xeroderma pigmentosum group G

MONDO:0010216

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

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

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Part of

↑ Xeroderma pigmentosum (6) ↑ Xeroderma pigmentosum-Cockayne syndrome complex (2) ↑ COFS syndrome (1)

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

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