Fanconi Anemia Complementation Group B
Disease ID: disease_node_15286
Connections displayed (default: 10).
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| Dbxref | MIM:300514 |
|---|---|
| Subclassof | DOID_0080012, DOID_13636 |
| Data Source | DOID |
| Synonyms | FACB, FANCB, Fanconi pancytopenia type 2 |
| Doid Label | Fanconi anemia complementation group B |
| Doid Description | A Fanconi anemia that has_material_basis_in mutation in the FANCB gene on chromosome Xp22. |
| Has Material Basis In | GENO_0000149 |
| Disease Node Id | disease_node_15286 |
| Doid Id | DOID_0111098 |
| Label | Fanconi Anemia Complementation Group B |
- Outgoing r'ship
SUBCLASS_OFto/from Fanconi Anemia(ID:disease_node_3172) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from X-Linked Recessive Disease(ID:disease_node_13254) (Disease)