Congenital Nonspherocytic Hemolytic Anemia 10
Disease ID: disease_node_15262
Connections displayed (default: 10).
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| Dbxref | MIM:618660 |
|---|---|
| Subclassof | DOID_2861 |
| Data Source | DOID |
| Doid Label | congenital nonspherocytic hemolytic anemia 10 |
| Doid Description | A congenital nonspherocytic hemolytic anemia that has_material_basis_in homozygous or compound heterozygous mutation in the GSR gene on chromosome 8p21. |
| Disease Node Id | disease_node_15262 |
| Doid Id | DOID_0051009 |
| Label | Congenital Nonspherocytic Hemolytic Anemia 10 |
- Outgoing r'ship
SUBCLASS_OFto/from Anemia, Hemolytic, Congenital Nonspherocytic(ID:disease_node_1189) (Disease)