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

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

Follow this condition — get notified about new trials

Broader categories

Sort by