Table S1.
Included diagnoses
| Included diagnoses | ICD-10 code |
|---|---|
| Hereditary hemolysis | |
| Enzyme deficiencies | D55 |
| (G6PD) deficiency, (PK) deficiency and others | |
| Hemoglobinopathies | |
| Thalassemia | D56 |
| Alpha-/Beta-thalassemia, thalassemia trait | |
| Sickle cell anemia | D57, M140c, N082c, H368c, M904 |
| Other hemoglobinopathies | D582 |
| Erythrocyte membrane defects | |
| Hereditary spherocytosis | D580 |
| Hereditary elliptocytosis | D581 |
| Hereditary stomatocytosis | D588a |
| Other hereditary hemolytic anemia | D588, D589 |
| Acquired hemolysis | |
| Autoimmune hemolytic anemia | D591 |
| Drug-induced immune and nonimmune hemolysis | D590, D592 |
| Cold-agglutinin disease | D591a |
| Cold hemoglobinuria | D596a |
| Other nonimmune hemolysis | D594, D594c |
| Paroxysmal nocturnal hemoglobinuria | D595 |
Note: The lowercase suffix is a specific Danish implementation of ICD-10 using lowercase letters to denote subtypes.
Abbreviations: G6PD, glucose-6-phosphate dehydrogenase; PK, Pyruvate kinase; ICD-10, International Classification of Diseases Tenth Revision.