Xeroderma pigmentosum group B
Xeroderma pigmentosum group B
Definition
Any xeroderma pigmentosum in which the cause of the disease is a mutation in the ERCC3 gene.
Also known as ERCC3 xeroderma pigmentosum, xeroderma pigmentosum caused by mutation in ERCC3, xeroderma pigmentosum group B, xeroderma pigmentosum group type B, xeroderma pigmentosum, complementation group type B, xeroderma pigmentosum, group B, XP-B, XP, Group B, XPB, XPBC — per MONDO
Also identified as
- DOID 0110850 per MONDO
- MESH C562590 per MONDO
- NCIT C3966 per MONDO
- OMIM 610651 per MONDO
- Orphanet 276252 per MONDO
- SCTID 1073003 per MONDO
- UMLS C0268136 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Integumental system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Skin of body | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |