Fanconi Anemia Complementation Group W
Disease ID: disease_node_15306
Connections displayed (default: 10).
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| Dbxref | MIM:617784 |
|---|---|
| Subclassof | DOID_0050737, DOID_13636 |
| Data Source | DOID |
| Doid Label | Fanconi anemia complementation group W |
| Doid Description | A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the RFWD3 gene on chromosome 16q23. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_15306 |
| Doid Id | DOID_0060978 |
| Label | Fanconi Anemia Complementation Group W |
- 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)