Fanconi Anemia Complementation Group U
Disease ID: disease_node_15299
Connections displayed (default: 10).
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| Dbxref | MIM:617247 |
|---|---|
| Subclassof | DOID_0050737, DOID_13636 |
| Data Source | DOID |
| Synonyms | FANCU |
| Doid Label | Fanconi anemia complementation group U |
| Doid Description | A Fanconi anemia that has_material_basis_in homozygous mutation in the XRCC2 gene on chromosome 7q36. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_15299 |
| Doid Id | DOID_0111085 |
| Label | Fanconi Anemia Complementation Group U |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Fanconi Anemia(ID:disease_node_3172) (Disease)