Symbol
| XPG
|
Location
| 13q33.1
|
Name
|
xeroderma pigmentosum, complementation group G |
Other name(s)
|
xeroderma pigmentosum VII |
Corresponding gene
|
ERCC5
|
Other symbol(s)
| XPGC, XP7
|
Main clinical features
|
with/without Cockayne syndrome, XP/CS complex
characterized by developmental retardation, dwarfism and severe neurologic abnormalities plus sun sensitivity and other abnormalities of XP |
Genetic determination
Related entries
| including skin cancer, severe form of cockayne with early onset
|
Function/system disorder
| dermatology |
Type
| disease
| |