Fanconi Anemia Complementation Group G
Disease ID: disease_node_15298
Connections displayed (default: 10).
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| Dbxref | MIM:614082 |
|---|---|
| Subclassof | DOID_0050177, DOID_13636 |
| Data Source | DOID |
| Synonyms | FANCG |
| Doid Label | Fanconi anemia complementation group G |
| Doid Description | A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the XRCC9 gene on chromosome 9p13. |
| Disease Node Id | disease_node_15298 |
| Doid Id | DOID_0111086 |
| Disease Has Basis In | SO_0000704 |
| Label | Fanconi Anemia Complementation Group G |
- Outgoing r'ship
SUBCLASS_OFto/from Fanconi Anemia(ID:disease_node_3172) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Monogenic Disease(ID:disease_node_13650) (Disease)