xeroderma pigmentosum group G (Q32143789)
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xeroderma pigmentosum that has material basis in homozygous or compound heterozygous mutation in the ERCC5 gene on chromosome 13q33
- XP7
- xeroderma pigmentosum VII
- XPG
- XP group G
- XP-G
- xeroderma pigmentosum, complementation group G
- Xeroderma Pigmentosum, Complementation Group type G
- Xp, Group G
- Xeroderma Pigmentosum 7
- Xeroderma Pigmentosum, Type G/Cockayne Syndrome
- XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG
- xeroderma pigmentosum group type G
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | xeroderma pigmentosum group G |
xeroderma pigmentosum that has material basis in homozygous or compound heterozygous mutation in the ERCC5 gene on chromosome 13q33 |
|
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