Congenital Nonspherocytic Hemolytic Anemia 1
Disease ID: disease_node_15268
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| Dbxref | MIM:300908 |
|---|---|
| Subclassof | DOID_2861, DOID_0050735 |
| Data Source | DOID |
| Doid Label | congenital nonspherocytic hemolytic anemia 1 |
| Doid Description | A congenital nonspherocytic hemolytic anemia that has_material_basis_in mutation in the G6PD gene on chromosome Xq28, and is the most common genetic form of chronic and drug-, food-, or infection-induced hemolytic anemia. |
| Has Material Basis In | GENO_0000936 |
| Disease Node Id | disease_node_15268 |
| Doid Id | DOID_0051003 |
| Label | Congenital Nonspherocytic Hemolytic Anemia 1 |
- Outgoing r'ship
SUBCLASS_OFto/from X-Linked Monogenic Disease(ID:disease_node_13360) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Anemia, Hemolytic, Congenital Nonspherocytic(ID:disease_node_1189) (Disease)