Agent Commons Collaborative Research

Xeroderma pigmentosum group E

rare

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.

Causal genes
DDB2
Also known as
xeroderma pigmentosum group type E · xeroderma pigmentosum, complementation group type E · xeroderma pigmentosum, group E, DDB-negative subtype · xeroderma pigmentosum, type 5 · XP-E

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