Xeroderma pigmentosum group D

MONDO:0010212

Any xeroderma pigmentosum in which the cause of the disease is a mutation in the ERCC2 gene.

Also known as: ERCC2 xeroderma pigmentosum, XP-D, XP4, XPD, XPDC, xeroderma pigmentosum caused by mutation in ERCC2, xeroderma pigmentosum group D, xeroderma pigmentosum group type D

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

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Where it sits in the disease tree

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Part of

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

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

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