Xeroderma pigmentosum group F
Xeroderma pigmentosum group F
Definition
Any xeroderma pigmentosum in which the cause of the disease is a mutation in the ERCC4 gene.
Also known as ERCC4 xeroderma pigmentosum, xeroderma pigmentosum caused by mutation in ERCC4, xeroderma pigmentosum group F, xeroderma pigmentosum group type F, xeroderma pigmentosum, complementation group type F, xeroderma pigmentosum, group F, XP-F, XP, group F, XP6, XPF — per MONDO
Also identified as
- DOID 0110848 per MONDO
- MESH C562592 per MONDO
- NCIT C3968 per MONDO
- OMIM 278760 per MONDO
- Orphanet 276264 per MONDO
- SCTID 42530008 per MONDO
- UMLS C0268140 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 |