xeroderma pigmentosum group F (Q32143775)
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xeroderma pigmentosum characterized by milder symptoms and later onset of skin cancer that has material basis in homozygous or compound heterozygous mutation in the ERCC4 gene on chromosome 16p13
- xeroderma pigmentosum VI
- XPF
- XP group F
- XP6
- xeroderma pigmentosum, complementation group F
- Xp, Group F
- xeroderma pigmentosum group type F
- Xeroderma Pigmentosum, Complementation Group type F
- XP-F
- Xeroderma Pigmentosum 6
- XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF
- Xeroderma Pigmentosum, Type F/Cockayne Syndrome
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | xeroderma pigmentosum group F |
xeroderma pigmentosum characterized by milder symptoms and later onset of skin cancer that has material basis in homozygous or compound heterozygous mutation in the ERCC4 gene on chromosome 16p13 |
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