Fanconi Anemia Complementation Group N
Disease ID: disease_node_15290
Connections displayed (default: 10).
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| Dbxref | MIM:610832 |
|---|---|
| Subclassof | DOID_0050177, DOID_13636 |
| Data Source | DOID |
| Synonyms | FANCN |
| Doid Label | Fanconi anemia complementation group N |
| Doid Description | A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the PALB2 gene on chromosome 16p12. |
| Disease Node Id | disease_node_15290 |
| Doid Id | DOID_0111094 |
| Disease Has Basis In | SO_0000704 |
| Label | Fanconi Anemia Complementation Group N |
- Outgoing r'ship
SUBCLASS_OFto/from Monogenic Disease(ID:disease_node_13650) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Fanconi Anemia(ID:disease_node_3172) (Disease)