Xeroderma Pigmentosum Group F
Disease ID: disease_node_20378
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:Q82.1, MIM:278760 |
|---|---|
| Subclassof | DOID_0050427 |
| Data Source | DOID |
| Synonyms | XP group F, XP6, XPF, xeroderma pigmentosum VI |
| Doid Label | xeroderma pigmentosum group F |
| Doid Description | A 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. |
| Disease Node Id | disease_node_20378 |
| Doid Id | DOID_0110848 |
| Label | Xeroderma Pigmentosum Group F |
- Outgoing r'ship
SUBCLASS_OFto/from Xeroderma Pigmentosum(ID:disease_node_8034) (Disease)