(Q32143748)
English
xeroderma pigmentosum group E
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.
- XPE
- xeroderma pigmentosum V
- XP group E
- XP5
- xeroderma pigmentosum, complementation group E
- Xeroderma Pigmentosum 5
- Xp, Group E
- XP-E
- Xeroderma Pigmentosum, Complementation Group type E
- xeroderma pigmentosum group type E
Statements
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C114771
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Identifiers
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