xeroderma pigmentosum group B (Q32143803)
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xeroderma pigmentosum characterized by that has material basis in mutation in the ERCC3 gene on chromosome 2q14
- XPBC
- XPB
- XP group B
- xeroderma pigmentosum, complementation group B
- Xpb/Cs
- Xeroderma Pigmentosum B/Cockayne Syndrome
- XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B; XPB
- Xeroderma Pigmentosum, Complementation Group type B
- xeroderma pigmentosum group type B
- XP-B
- Xp, Group B
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | xeroderma pigmentosum group B |
xeroderma pigmentosum characterized by that has material basis in mutation in the ERCC3 gene on chromosome 2q14 |
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Statements
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