Xeroderma pigmentosum group B

MONDO:0012531

Any xeroderma pigmentosum in which the cause of the disease is a mutation in the ERCC3 gene.

Also known as: ERCC3 xeroderma pigmentosum, XP, Group B, XP-B, XPB, XPBC, xeroderma pigmentosum caused by mutation in ERCC3, xeroderma pigmentosum group B, xeroderma pigmentosum group type B

3 clinical trials for this condition and its sub-types, 0 tagged with Xeroderma pigmentosum group B 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 B (0)

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