Xeroderma pigmentosum group E

MONDO:0010213

An autosomal recessive genetic disorder caused by mutations in the DDB2 gene. This disease exhibits the mildest degree of sun sensitivity of all xeroderma pigmentosum complementation groups, although individuals are at high risk for skin cancer.

Also known as: XP-E, XP5, XPE, xeroderma pigmentosum group E, xeroderma pigmentosum group type E, xeroderma pigmentosum, complementation group type E, xeroderma pigmentosum, group E, DDB-negative subtype, XP, Group E

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

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↑ Xeroderma pigmentosum (6)

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

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