Heinz Body Anemia
Disease ID: disease_node_15261
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| Dbxref | GARD:10718, MIM:140700 |
|---|---|
| Subclassof | DOID_0050736, DOID_2861 |
| Data Source | DOID |
| Doid Label | Heinz body anemia |
| Doid Description | A congenital nonspherocytic hemolytic anemia characterized by nonspherocytic hemolytic anemia of Dacie type I with Heinz bodies seen in erythrocytes after splenectomy that has_material_basis_in heterozygous mutation in the HBA1, HBA2 or HBB genes on chromosome 11p15.4, 16p13.3, and 16p13.3, respectively. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_15261 |
| Doid Id | DOID_0111363 |
| Label | Heinz Body Anemia |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Anemia, Hemolytic, Congenital Nonspherocytic(ID:disease_node_1189) (Disease)