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. 2016 Jun 24;8:241–252. doi: 10.2147/CLEP.S93643

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.