Xeroderma Pigmentosum Group G
Disease ID: disease_node_20377
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| Dbxref | ICD10CM:Q82.1, MIM:278780 |
|---|---|
| Subclassof | DOID_0050427 |
| Data Source | DOID |
| Synonyms | XP group G, XP7, XPG, xeroderma pigmentosum VII |
| Doid Label | xeroderma pigmentosum group G |
| Doid Description | A xeroderma pigmentosum that has_material_basis_in homozygous or compound heterozygous mutation in the ERCC5 gene on chromosome 13q33. |
| Disease Node Id | disease_node_20377 |
| Doid Id | DOID_0110849 |
| Label | Xeroderma Pigmentosum Group G |
- Outgoing r'ship
SUBCLASS_OFto/from Xeroderma Pigmentosum(ID:disease_node_8034) (Disease)