Table S1.
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.