Congenital Nonspherocytic Hemolytic Anemia 5
Disease ID: disease_node_15265
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| Dbxref | MIM:235700 |
|---|---|
| Subclassof | DOID_2861, DOID_0050737 |
| Data Source | DOID |
| Doid Label | congenital nonspherocytic hemolytic anemia 5 |
| Doid Description | A congenital nonspherocytic hemolytic anemia that has_material_basis_in homozygous or compound heterozygous mutation in the HK1 gene, which encodes a form of hexokinase, on chromosome 10q22. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_15265 |
| Doid Id | DOID_0051006 |
| Label | Congenital Nonspherocytic Hemolytic Anemia 5 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Anemia, Hemolytic, Congenital Nonspherocytic(ID:disease_node_1189) (Disease)