| Source | Code | Name | Case count | Share of cases (%) |
|---|---|---|---|---|
| OUTPAT | OUTPAT_ICD10(D649) | Anaemia, unspecified | 9166 | |
| OUTPAT | OUTPAT_ICD10(D509) | Iron deficiency anaemia, unspecified | 6523 | |
| INPAT | INPAT_ICD10(D649) | Anaemia, unspecified | 5378 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D649) | Anaemia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 4895 | |
| INPAT | INPAT_ICD10(D509) | Iron deficiency anaemia, unspecified | 3297 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D509) | Iron deficiency anaemia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 3001 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D50) | Iron deficiency anaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 1637 | |
| INPAT | INPAT_ICD10(D7082) | Drug-induced neutropenia | 1531 | |
| OUTPAT | OUTPAT_ICD10(D696) | Thrombocytopenia, unspecified | 1329 | |
| OUTPAT | OUTPAT_ICD10(D860) | Sarcoidosis of lung | 1258 | |
| OUTPAT | OUTPAT_ICD10(D7082) | Drug-induced neutropenia | 1040 | |
| REIMB | REIMB_KELA(107)_ICD10(D51) | Pernicious anaemia, Vitamin B12deficiency anaemia | 1032 | |
| OUTPAT | OUTPAT_ICD10(D7089) | Neutropenic splenomegaly | 979 | |
| OUTPAT | OUTPAT_ICD10(D868) | Sarcoidosis of other and combined sites | 911 | |
| OUTPAT | OUTPAT_ICD10(D862) | Sarcoidosis of lung with sarcoidosis of lymph nodes | 864 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D648) | Other specified anaemias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 801 | |
| OUTPAT | OUTPAT_ICD10(D688) | Other specified coagulation defects | 782 | |
| OUTPAT | OUTPAT_ICD10(D728) | Other specified disorders of white blood cells | 740 | |
| OUTPAT | OUTPAT_ICD10(D869) | Sarcoidosis, unspecified | 725 | |
| INPAT | INPAT_ICD10(D696) | Thrombocytopenia, unspecified | 723 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D508) | Other iron deficiency anaemias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 706 | |
| OUTPAT | OUTPAT_ICD10(D693) | Idiopathic thrombocytopenic purpura | 605 | |
| OUTPAT | OUTPAT_ICD10(D690) | Allergic purpura | 597 | |
| OUTPAT | OUTPAT_ICD10(D508) | Other iron deficiency anaemias | 594 | |
| OUTPAT | OUTPAT_ICD10(D752) | Essential thrombocytosis | 586 | |
| INPAT | INPAT_ICD10(D62) | Acute posthaemorrhagic anaemia | 580 | |
| OUTPAT | OUTPAT_ICD10(D861) | Sarcoidosis of lymph nodes | 578 | |
| INPAT | INPAT_ICD10(D7089) | Neutropenic splenomegaly | 540 | |
| OUTPAT | OUTPAT_ICD10(D8980) | Immunoglobulin A (IgA) deposits in organisms | 540 | |
| OUTPAT | OUTPAT_ICD10(D751) | Secondary polycythaemia | 485 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D519) | Vitamin B12deficiency anaemia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 474 | |
| OUTPAT | OUTPAT_ICD10(D519) | Vitamin B12deficiency anaemia, unspecified | 466 | |
| OUTPAT | OUTPAT_ICD10(D648) | Other specified anaemias | 457 | |
| OUTPAT | OUTPAT_ICD10(D62) | Acute posthaemorrhagic anaemia | 430 | |
| OUTPAT | OUTPAT_ICD10(D759) | Disease of blood and blood-forming organs, unspecified | 429 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D51) | Vitamin B12deficiency anaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 418 | |
| INPAT | INPAT_ICD8(13597) | Sarcoidosis, Suspecta | 410 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D696) | Thrombocytopenia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 387 | |
| INPAT | INPAT_ICD10(D860) | Sarcoidosis of lung | 385 | |
| INPAT | INPAT_ICD10(D693) | Idiopathic thrombocytopenic purpura | 381 | |
| INPAT | INPAT_ICD10(D688) | Other specified coagulation defects | 369 | |
| INPAT | INPAT_ICD10(D868) | Sarcoidosis of other and combined sites | 364 | |
| INPAT | INPAT_ICD8(13599) | Sarcoidosis, Unspecified | 353 | |
| INPAT | INPAT_ICD10(D519) | Vitamin B12deficiency anaemia, unspecified | 338 | |
| OUTPAT | OUTPAT_ICD10(D510) | Vitamin B12deficiency anaemia due to intrinsic factor deficiency | 338 | |
| OUTPAT | OUTPAT_ICD10(D638) | Anaemia in other chronic diseases classified elsewhere | 323 | |
| OUTPAT | OUTPAT_ICD10(D721) | Eosinophilia | 320 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D688) | Other specified coagulation defects. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 316 | |
| INPAT | INPAT_ICD9(1350A) | Sarcoidosis | 313 | |
| INPAT | INPAT_ICD10(D8980) | Immunoglobulin A (IgA) deposits in organisms | 307 | |
| REIMB | REIMB_KELA(107)_ICD9(NA) | Pernicious anaemia, Name not found | 281 | |
| REIMB | REIMB_KELA(132)_ICD10(D86) | Sarcoidosis, Sarcoidosis | 279 | |
| OUTPAT | OUTPAT_ICD10(D699) | Haemorrhagic condition, unspecified | 272 | |
| OUTPAT | OUTPAT_ICD10(D680) | Von Willebrand's disease | 267 | |
| INPAT | INPAT_ICD10(D648) | Other specified anaemias | 264 | |
| OUTPAT | OUTPAT_ICD10(D50) | Iron deficiency anaemia | 260 | |
| REIMB | REIMB_KELA(107)_ICD10(E538) | Pernicious anaemia, Deficiency of other specified B group vitamins | 256 | |
| OUTPAT | OUTPAT_ICD10(D689) | Coagulation defect, unspecified | 249 | |
| OUTPAT | OUTPAT_ICD10(D801) | Nonfamilial hypogammaglobulinaemia | 246 | |
| OUTPAT | OUTPAT_ICD10(D863) | Sarcoidosis of skin | 244 | |
| INPAT | INPAT_ICD9(2809X) | Iron deficiency anemia, unspecified | 242 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D510) | Vitamin B12deficiency anaemia due to intrinsic factor deficiency. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 239 | |
| INPAT | INPAT_ICD10(D869) | Sarcoidosis, unspecified | 238 | |
| INPAT | INPAT_ICD10(D690) | Allergic purpura | 210 | |
| INPAT | INPAT_ICD9(2859X) | Other and unspecified anaemias, Anaemia, unspecified | 205 | |
| OUTPAT | OUTPAT_ICD10(D591) | Other autoimmune haemolytic anaemias | 203 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D752) | Essential thrombocytosis. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 201 | |
| INPAT | INPAT_ICD10(D510) | Vitamin B12deficiency anaemia due to intrinsic factor deficiency | 190 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D64) | Other anaemias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 189 | |
| OUTPAT | OUTPAT_ICD10(D809) | Immunodeficiency with predominantly antibody defects, unspecified | 187 | |
| INPAT | INPAT_ICD10(D508) | Other iron deficiency anaemias | 186 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D62) | Acute posthaemorrhagic anaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 183 | |
| OUTPAT | OUTPAT_ICD10(D682) | Hereditary deficiency of other clotting factors | 179 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D860) | Sarcoidosis of lung. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 179 | |
| REIMB | REIMB_KELA(132)_ICD8(NA) | Sarcoidosis, Name not found | 176 | |
| INPAT | INPAT_ICD10(D638) | Anaemia in other chronic diseases classified elsewhere | 175 | |
| INPAT | INPAT_ICD10(D862) | Sarcoidosis of lung with sarcoidosis of lymph nodes | 174 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D8980) | Immunoglobulin A (IgA) deposits in organisms. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 167 | |
| OUTPAT | OUTPAT_ICD10(D803) | Selective deficiency of immunoglobulin G [IgG] subclasses | 166 | |
| INPAT | INPAT_ICD10(D680) | Von Willebrand's disease | 163 | |
| INPAT | INPAT_ICD10(D695) | Secondary thrombocytopenia | 160 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D868) | Sarcoidosis of other and combined sites. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 160 | |
| OUTPAT | OUTPAT_ICD10(D692) | Other nonthrombocytopenic purpura | 159 | |
| REIMB | REIMB_KELA(107)_ICD10(C16) | Pernicious anaemia, Malignant neoplasm of stomach | 158 | |
| INPAT | INPAT_ICD10(D591) | Other autoimmune haemolytic anaemias | 153 | |
| INPAT | INPAT_ICD10(D752) | Essential thrombocytosis | 152 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D728) | Other specified disorders of white blood cells. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 141 | |
| OUTPAT | OUTPAT_ICD10(D808) | Other immunodeficiencies with predominantly antibody defects | 140 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D7089) | Neutropenic splenomegaly. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 140 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D690) | Allergic purpura. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 135 | |
| INPAT | INPAT_ICD10(D728) | Other specified disorders of white blood cells | 134 | |
| OUTPAT | OUTPAT_ICD10(D599) | Acquired haemolytic anaemia, unspecified | 134 | |
| OUTPAT | OUTPAT_ICD10(D729) | Disorder of white blood cells, unspecified | 134 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D86) | Sarcoidosis. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 132 | |
| DEATH | DEATH_ICD10(D683) | Haemorrhagic disorder due to circulating anticoagulants | 129 | |
| REIMB | REIMB_KELA(107)_ICD8(NA) | Pernicious anaemia, Name not found | 129 | |
| INPAT | INPAT_ICD10(D801) | Nonfamilial hypogammaglobulinaemia | 125 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D638) | Anaemia in other chronic diseases classified elsewhere. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 123 | |
| INPAT | INPAT_ICD10(D721) | Eosinophilia | 122 | |
| OUTPAT | OUTPAT_ICD10(D695) | Secondary thrombocytopenia | 122 | |
| REIMB | REIMB_KELA(107)_ICD10(D510) | Pernicious anaemia, Vitamin B12deficiency anaemia due to intrinsic factor deficiency | 122 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D693) | Idiopathic thrombocytopenic purpura. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 121 | |
| OUTPAT | OUTPAT_ICD10(D750) | Familial erythrocytosis | 120 | |
| OUTPAT | OUTPAT_ICD10(D531) | Other megaloblastic anaemias, not elsewhere classified | 119 | |
| INPAT | INPAT_ICD8(28700) | Purpura and other haemorrhagic conditions, Allergic purpura | 113 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D699) | Haemorrhagic condition, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 113 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D518) | Other vitamin B12deficiency anaemias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 108 | |
| INPAT | INPAT_ICD10(D861) | Sarcoidosis of lymph nodes | 104 | |
| OUTPAT | OUTPAT_ICD10(D683) | Haemorrhagic disorder due to circulating anticoagulants | 97 | |
| OUTPAT | OUTPAT_ICD10(D619) | Aplastic anaemia, unspecified | 93 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D862) | Sarcoidosis of lung with sarcoidosis of lymph nodes. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 92 | |
| INPAT | INPAT_ICD10(D682) | Hereditary deficiency of other clotting factors | 91 | |
| INPAT | INPAT_ICD10(D735) | Infarction of spleen | 87 | |
| INPAT | INPAT_ICD10(D599) | Acquired haemolytic anaemia, unspecified | 86 | |
| INPAT | INPAT_ICD8(28719) | Purpura and other haemorrhagic conditions, Thrombocytopenia NUD | 84 | |
| REIMB | REIMB_KELA(132)_ICD9(NA) | Sarcoidosis, Name not found | 84 | |
| OUTPAT | OUTPAT_ICD10(D691) | Qualitative platelet defects | 82 | |
| OUTPAT | OUTPAT_ICD10(D731) | Hypersplenism | 82 | |
| INPAT | INPAT_ICD10(D50) | Iron deficiency anaemia | 81 | |
| OUTPAT | OUTPAT_ICD10(D800) | Hereditary hypogammaglobulinaemia | 81 | |
| INPAT | INPAT_ICD9(2851A) | Acute posthemorrhagic anemia | 80 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D698) | Other specified haemorrhagic conditions. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 80 | |
| INPAT | INPAT_ICD10(D531) | Other megaloblastic anaemias, not elsewhere classified | 79 | |
| OUTPAT | OUTPAT_ICD10(D802) | Selective deficiency of immunoglobulin A [IgA] | 79 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D751) | Secondary polycythaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 79 | |
| INPAT | INPAT_ICD10(D699) | Haemorrhagic condition, unspecified | 78 | |
| OUTPAT | OUTPAT_ICD10(D8989) | Other specified disorders involving the immune mechanism, not elsewhere classified | 75 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D729) | Disorder of white blood cells, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 73 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D69) | Purpura and other haemorrhagic conditions. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 71 | |
| OUTPAT | OUTPAT_ICD10(D735) | Infarction of spleen | 70 | |
| REIMB | REIMB_KELA(107)_ICD10(D519) | Pernicious anaemia, Vitamin B12deficiency anaemia, unspecified | 70 | |
| OUTPAT | OUTPAT_ICD10(D814) | Nezelof's syndrome | 69 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D689) | Coagulation defect, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 69 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D869) | Sarcoidosis, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 68 | |
| DEATH | DEATH_ICD10(D649) | Anaemia, unspecified | 67 | |
| OUTPAT | OUTPAT_ICD10(D8418) | Other specified defect in the complement system | 67 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D680) | Von Willebrand's disease. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 66 | |
| INPAT | INPAT_ICD10(D630) | Anaemia in neoplastic disease (C00-D48+) | 65 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D7082) | Drug-induced neutropenia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 65 | |
| OUTPAT | OUTPAT_ICD10(D694) | Other primary thrombocytopenia | 63 | |
| REIMB | REIMB_KELA(120)_ICD10(D80) | Hypogammaglobulinaemia, Immunodeficiency with predominantly antibody defects | 63 | |
| INPAT | INPAT_ICD10(D619) | Aplastic anaemia, unspecified | 61 | |
| INPAT | INPAT_ICD10(D683) | Haemorrhagic disorder due to circulating anticoagulants | 60 | |
| INPAT | INPAT_ICD10(D689) | Coagulation defect, unspecified | 60 | |
| OUTPAT | OUTPAT_ICD10(D698) | Other specified haemorrhagic conditions | 60 | |
| OUTPAT | OUTPAT_ICD10(D849) | Immunodeficiency, unspecified | 60 | |
| INPAT | INPAT_ICD10(D810) | Severe combined immunodeficiency [SCID] with reticular dysgenesis | 59 | |
| INPAT | INPAT_ICD8(28599) | Other and unspecified anaemias, Anaemia, unspecified | 59 | |
| INPAT | INPAT_ICD10(D809) | Immunodeficiency with predominantly antibody defects, unspecified | 58 | |
| INPAT | INPAT_ICD9(2870A) | Purpura and other haemorrhagic conditions, Allergic purpura | 58 | |
| OUTPAT | OUTPAT_ICD10(D66) | Hereditary factor VIII deficiency | 58 | |
| INPAT | INPAT_ICD10(D65) | Disseminated intravascular coagulation [defibrination syndrome] | 57 | |
| INPAT | INPAT_ICD10(D759) | Disease of blood and blood-forming organs, unspecified | 57 | |
| OUTPAT | OUTPAT_ICD10(D830) | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function | 57 | |
| OUTPAT | OUTPAT_ICD10(D839) | Common variable immunodeficiency, unspecified | 57 | |
| INPAT | INPAT_ICD10(D814) | Nezelof's syndrome | 56 | |
| OUTPAT | OUTPAT_ICD10(D501) | Sideropenic dysphagia | 56 | |
| OUTPAT | OUTPAT_ICD10(D609) | Acquired pure red cell aplasia, unspecified | 56 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D682) | Hereditary deficiency of other clotting factors. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 56 | |
| OUTPAT | OUTPAT_ICD10(D640) | Hereditary sideroblastic anaemia | 55 | |
| INPAT | INPAT_ICD9(2810X) | Other deficiency anaemias, Pernicious anaemia | 54 | |
| OUTPAT | OUTPAT_ICD10(D529) | Folate deficiency anaemia, unspecified | 54 | |
| INPAT | INPAT_ICD9(2888B) | Diseases of white blood cells, Other specified disease of white blood cells | 53 | |
| OUTPAT | OUTPAT_ICD10(D518) | Other vitamin B12deficiency anaemias | 53 | |
| OUTPAT | OUTPAT_ICD10(D758) | Other specified diseases of blood and blood-forming organs | 53 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D692) | Other nonthrombocytopenic purpura. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 53 | |
| OUTPAT | OUTPAT_ICD10(D643) | Other sideroblastic anaemias | 52 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D531) | Other megaloblastic anaemias, not elsewhere classified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 52 | |
| OUTPAT | OUTPAT_ICD10(D899) | Disorder involving the immune mechanism, unspecified | 51 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D759) | Disease of blood and blood-forming organs, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 51 | |
| OUTPAT | OUTPAT_ICD10(D841) | Defects in the complement system | 49 | |
| REIMB | REIMB_KELA(107)_ICD10(NA) | Pernicious anaemia, Name not found | 49 | |
| INPAT | INPAT_ICD10(D529) | Folate deficiency anaemia, unspecified | 48 | |
| INPAT | INPAT_ICD10(D803) | Selective deficiency of immunoglobulin G [IgG] subclasses | 48 | |
| OUTPAT | OUTPAT_ICD10(D593) | Haemolytic-uraemic syndrome | 48 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D861) | Sarcoidosis of lymph nodes. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 47 | |
| INPAT | INPAT_ICD10(D751) | Secondary polycythaemia | 46 | |
| OUTPAT | OUTPAT_ICD10(D630) | Anaemia in neoplastic disease (C00-D48+) | 46 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D721) | Eosinophilia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 46 | |
| REIMB | REIMB_KELA(132)_ICD10(D868) | Sarcoidosis, Sarcoidosis of other and combined sites | 46 | |
| OUTPAT | OUTPAT_ICD10(D8419) | Unspecified defect in the complement system | 45 | |
| INPAT | INPAT_ICD10(D640) | Hereditary sideroblastic anaemia | 44 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D801) | Nonfamilial hypogammaglobulinaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 43 | |
| REIMB | REIMB_KELA(107)_ICD9(281) | Pernicious anaemia, Other deficiency anaemias | 43 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D591) | Other autoimmune haemolytic anaemias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 42 | |
| INPAT | INPAT_ICD10(D731) | Hypersplenism | 41 | |
| INPAT | INPAT_ICD8(28899) | Agranulocytosis | 40 | |
| OUTPAT | OUTPAT_ICD10(D580) | Hereditary spherocytosis | 40 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D529) | Folate deficiency anaemia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 40 | |
| REIMB | REIMB_KELA(120)_ICD10(D801) | Hypogammaglobulinaemia, Nonfamilial hypogammaglobulinaemia | 40 | |
| OUTPAT | OUTPAT_ICD10(D7080) | Agranulocytic angina | 39 | |
| INPAT | INPAT_ICD10(D643) | Other sideroblastic anaemias | 38 | |
| INPAT | INPAT_ICD8(28590) | Other and unspecified anaemias, Secundaria (e nephropatia, collagenosa, infectione etc.) | 38 | |
| OUTPAT | OUTPAT_ICD10(D582) | Other haemoglobinopathies | 38 | |
| OUTPAT | OUTPAT_ICD10(D610) | Constitutional aplastic anaemia | 38 | |
| INPAT | INPAT_ICD9(2859A) | Other and unspecified anaemias, Anaemia, unspecified | 37 | |
| INPAT | INPAT_ICD9(2875A) | Thrombocytopenia, unspecified | 37 | |
| OUTPAT | OUTPAT_ICD10(D739) | Disease of spleen, unspecified | 37 | |
| INPAT | INPAT_ICD9(2808X) | Other specified iron deficiency anemias | 36 | |
| OUTPAT | OUTPAT_ICD10(D65) | Disseminated intravascular coagulation [defibrination syndrome] | 36 | |
| INPAT | INPAT_ICD10(D808) | Other immunodeficiencies with predominantly antibody defects | 35 | |
| OUTPAT | OUTPAT_ICD10(D613) | Idiopathic aplastic anaemia | 35 | |
| REIMB | REIMB_KELA(132)_ICD10(D862) | Sarcoidosis, Sarcoidosis of lung with sarcoidosis of lymph nodes | 35 | |
| OUTPAT | OUTPAT_ICD10(D641) | Secondary sideroblastic anaemia due to disease | 34 | |
| OUTPAT | OUTPAT_ICD10(D734) | Cyst of spleen | 34 | |
| REIMB | REIMB_KELA(107)_ICD9(2810X) | Pernicious anaemia, Other deficiency anaemias, Pernicious anaemia | 34 | |
| INPAT | INPAT_ICD10(D66) | Hereditary factor VIII deficiency | 33 | |
| INPAT | INPAT_ICD10(D8989) | Other specified disorders involving the immune mechanism, not elsewhere classified | 32 | |
| OUTPAT | OUTPAT_ICD10(D594) | Other nonautoimmune haemolytic anaemias | 32 | |
| OUTPAT | OUTPAT_ICD10(D684) | Acquired coagulation factor deficiency | 32 | |
| OUTPAT | OUTPAT_ICD10(D806) | Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia | 32 | |
| OUTPAT | OUTPAT_ICD10(D898) | Name not found | 32 | |
| INPAT | INPAT_ICD8(28900) | Other disease of blood and blood-forming organs, Polycythaemia, secondary | 31 | |
| INPAT | INPAT_ICD9(2801A) | Iron deficiency anemia secondary to inadequate dietary iron intake | 31 | |
| OUTPAT | OUTPAT_ICD10(D7081) | Neutropenia congenital | 31 | |
| INPAT | INPAT_ICD10(D593) | Haemolytic-uraemic syndrome | 30 | |
| INPAT | INPAT_ICD10(D839) | Common variable immunodeficiency, unspecified | 30 | |
| INPAT | INPAT_ICD8(28710) | Purpura and other haemorrhagic conditions, Thrombocytopenia essentialis (Morbus Werlhof) | 30 | |
| INPAT | INPAT_ICD8(28799) | Purpura and other haemorrhagic conditions, Other and unspecified | 30 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D803) | Selective deficiency of immunoglobulin G [IgG] subclasses. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 30 | |
| REIMB | REIMB_KELA(107)_ICD10(D518) | Pernicious anaemia, Other vitamin B12deficiency anaemias | 30 | |
| INPAT | INPAT_ICD10(D611) | Drug-induced aplastic anaemia | 29 | |
| INPAT | INPAT_ICD10(D729) | Disorder of white blood cells, unspecified | 29 | |
| OUTPAT | OUTPAT_ICD10(D810) | Severe combined immunodeficiency [SCID] with reticular dysgenesis | 29 | |
| INPAT | INPAT_ICD10(D501) | Sideropenic dysphagia | 28 | |
| INPAT | INPAT_ICD10(D739) | Disease of spleen, unspecified | 28 | |
| INPAT | INPAT_ICD10(D863) | Sarcoidosis of skin | 28 | |
| INPAT | INPAT_ICD8(28110) | Other vitamin B12 deficiency anaemia, Other vitamin B12 deficiency | 28 | |
| OUTPAT | OUTPAT_ICD10(D51) | Vitamin B12deficiency anaemia | 28 | |
| INPAT | INPAT_ICD10(D613) | Idiopathic aplastic anaemia | 27 | |
| OUTPAT | OUTPAT_ICD10(D539) | Nutritional anaemia, unspecified | 27 | |
| OUTPAT | OUTPAT_ICD10(D730) | Hyposplenism | 27 | |
| OUTPAT | OUTPAT_ICD10(D838) | Other common variable immunodeficiencies | 27 | |
| OUTPAT | OUTPAT_ICD10(D891) | Cryoglobulinaemia | 27 | |
| OUTPAT | OUTPAT_ICD10(D8982) | Disease caused by deposition of the light chain of the immunoglobulins | 27 | |
| INPAT | INPAT_ICD8(28998) | Other disease of blood and blood-forming organs, Alii definiti | 26 | |
| OUTPAT | OUTPAT_ICD10(D598) | Other acquired haemolytic anaemias | 26 | |
| INPAT | INPAT_ICD10(D802) | Selective deficiency of immunoglobulin A [IgA] | 25 | |
| INPAT | INPAT_ICD8(28199) | Other vitamin B12 deficiency anaemia, Other and unspecified deficiency anaemia | 25 | |
| INPAT | INPAT_ICD9(2864A) | Von Willebrand's disease | 25 | |
| INPAT | INPAT_ICD9(2880B) | Diseases of white blood cells, Agranulocytosis | 25 | |
| OUTPAT | OUTPAT_ICD10(D70) | Agranulocytosis | 25 | |
| OUTPAT | OUTPAT_ICD10(D763) | Other histiocytosis syndromes | 25 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D52) | Folate deficiency anaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 25 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D68) | Other coagulation defects. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 25 | |
| INPAT | INPAT_ICD10(D641) | Secondary sideroblastic anaemia due to disease | 24 | |
| INPAT | INPAT_ICD10(D692) | Other nonthrombocytopenic purpura | 24 | |
| INPAT | INPAT_ICD10(D694) | Other primary thrombocytopenia | 24 | |
| INPAT | INPAT_ICD8(28109) | Other anaemia, Perniciosa non definita | 24 | |
| OUTPAT | OUTPAT_ICD10(D8411) | Hereditary angioedema type I | 24 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D599) | Acquired haemolytic anaemia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 24 | |
| REIMB | REIMB_KELA(132)_ICD10(D860) | Sarcoidosis, Sarcoidosis of lung | 24 | |
| INPAT | INPAT_ICD10(D610) | Constitutional aplastic anaemia | 23 | |
| OUTPAT | OUTPAT_ICD10(D563) | Thalassaemia trait | 23 | |
| OUTPAT | OUTPAT_ICD10(D64) | Other anaemias | 23 | |
| OUTPAT | OUTPAT_ICD10(D738) | Other diseases of spleen | 23 | |
| OUTPAT | OUTPAT_ICD10(D7600) | Eosinophilic granuloma | 23 | |
| OUTPAT | OUTPAT_ICD10(D848) | Other specified immunodeficiencies | 23 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D808) | Other immunodeficiencies with predominantly antibody defects. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 23 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D809) | Immunodeficiency with predominantly antibody defects, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 23 | |
| INPAT | INPAT_ICD10(D691) | Qualitative platelet defects | 22 | |
| INPAT | INPAT_ICD10(D761) | Haemophagocytic lymphohistiocytosis | 22 | |
| INPAT | INPAT_ICD8(28630) | Coagulation defects, Vascular haemophilia | 22 | |
| OUTPAT | OUTPAT_ICD10(D831) | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders | 22 | |
| OUTPAT | OUTPAT_ICD10(D86) | Sarcoidosis | 22 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D643) | Other sideroblastic anaemias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 22 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D72) | Other disorders of white blood cells. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 22 | |
| REIMB | REIMB_KELA(107)_ICD10(C163) | Pernicious anaemia, Pyloric antrum | 22 | |
| INPAT | INPAT_ICD10(D518) | Other vitamin B12deficiency anaemias | 21 | |
| INPAT | INPAT_ICD10(D520) | Dietary folate deficiency anaemia | 21 | |
| INPAT | INPAT_ICD10(D580) | Hereditary spherocytosis | 21 | |
| INPAT | INPAT_ICD10(D609) | Acquired pure red cell aplasia, unspecified | 21 | |
| OUTPAT | OUTPAT_ICD10(D590) | Drug-induced autoimmune haemolytic anaemia | 21 | |
| OUTPAT | OUTPAT_ICD10(D818) | Other combined immunodeficiencies | 21 | |
| OUTPAT | OUTPAT_ICD10(D892) | Hypergammaglobulinaemia, unspecified | 21 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D750) | Familial erythrocytosis. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 21 | |
| REIMB | REIMB_KELA(122)_ICD10(D61) | Aplastic anaemia, Other aplastic anaemias | 21 | |
| INPAT | INPAT_ICD10(D7080) | Agranulocytic angina | 20 | |
| INPAT | INPAT_ICD10(D800) | Hereditary hypogammaglobulinaemia | 20 | |
| INPAT | INPAT_ICD8(28999) | Other disease of blood and blood-forming organs, Other and unspecified | 20 | |
| OUTPAT | OUTPAT_ICD10(D7601) | Histiocytosis X (chronic) | 20 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D695) | Secondary thrombocytopenia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 20 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D75) | Other diseases of blood and blood-forming organs. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 20 | |
| INPAT | INPAT_ICD10(D598) | Other acquired haemolytic anaemias | 19 | |
| INPAT | INPAT_ICD10(D7081) | Neutropenia congenital | 19 | |
| INPAT | INPAT_ICD9(2858X) | Other specified anemias | 19 | |
| OUTPAT | OUTPAT_ICD10(D561) | Beta thalassaemia | 19 | |
| OUTPAT | OUTPAT_ICD10(D5699) | Thalassaemia, unspecified | 19 | |
| OUTPAT | OUTPAT_ICD10(D573) | Sickle-cell trait | 19 | |
| OUTPAT | OUTPAT_ICD10(D611) | Drug-induced aplastic anaemia | 19 | |
| OUTPAT | OUTPAT_ICD10(D761) | Haemophagocytic lymphohistiocytosis | 19 | |
| OUTPAT | OUTPAT_ICD10(D819) | Combined immunodeficiency, unspecified | 19 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D683) | Haemorrhagic disorder due to circulating anticoagulants. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 19 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D863) | Sarcoidosis of skin. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 19 | |
| REIMB | REIMB_KELA(107)_ICD10(C162) | Pernicious anaemia, Body of stomach | 19 | |
| REIMB | REIMB_KELA(122)_ICD10(D619) | Aplastic anaemia, Aplastic anaemia, unspecified | 19 | |
| DEATH | DEATH_ICD10(D509) | Iron deficiency anaemia, unspecified | 18 | |
| INPAT | INPAT_ICD10(D539) | Nutritional anaemia, unspecified | 18 | |
| INPAT | INPAT_ICD10(D698) | Other specified haemorrhagic conditions | 18 | |
| INPAT | INPAT_ICD10(D738) | Other diseases of spleen | 18 | |
| INPAT | INPAT_ICD9(2790B) | Disorders involving the immune mechanism, Deficiency of humoral immunity | 18 | |
| OUTPAT | OUTPAT_ICD10(D520) | Dietary folate deficiency anaemia | 18 | |
| OUTPAT | OUTPAT_ICD10(D578) | Other sickle-cell disorders | 18 | |
| OUTPAT | OUTPAT_ICD10(D618) | Other specified aplastic anaemias | 18 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D630) | Anaemia in neoplastic disease (C00-D48+). Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 18 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D691) | Qualitative platelet defects. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 18 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D73) | Diseases of spleen. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 18 | |
| INPAT | INPAT_ICD10(D684) | Acquired coagulation factor deficiency | 17 | |
| INPAT | INPAT_ICD10(D806) | Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia | 17 | |
| INPAT | INPAT_ICD10(D849) | Immunodeficiency, unspecified | 17 | |
| INPAT | INPAT_ICD10(D899) | Disorder involving the immune mechanism, unspecified | 17 | |
| INPAT | INPAT_ICD8(28200) | Hereditary haemolytic anaemias, Familial acholuric jaundice | 17 | |
| INPAT | INPAT_ICD9(2790C) | Disorders involving the immune mechanism, Deficiency of humoral immunity | 17 | |
| INPAT | INPAT_ICD9(2811A) | Other vitamin B12 deficiency anemia | 17 | |
| INPAT | INPAT_ICD9(2860A) | Congenital factor VIII disorder | 17 | |
| OUTPAT | OUTPAT_ICD10(D595) | Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli] | 17 | |
| OUTPAT | OUTPAT_ICD10(D600) | Chronic acquired pure red cell aplasia | 17 | |
| OUTPAT | OUTPAT_ICD10(D890) | Polyclonal hypergammaglobulinaemia | 17 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D513) | Other dietary vitamin B12deficiency anaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 17 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D66) | Hereditary factor VIII deficiency. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 17 | |
| REIMB | REIMB_KELA(132)_ICD9(1350A) | Sarcoidosis, Sarcoidosis | 17 | |
| INPAT | INPAT_ICD10(D818) | Other combined immunodeficiencies | 16 | |
| INPAT | INPAT_ICD8(28600) | Coagulation defects, Haemophilia | 16 | |
| INPAT | INPAT_ICD9(2819X) | Unspecified deficiency anemia | 16 | |
| OUTPAT | OUTPAT_ICD10(D513) | Other dietary vitamin B12deficiency anaemia | 16 | |
| OUTPAT | OUTPAT_ICD10(D560) | Alpha thalassaemia | 16 | |
| OUTPAT | OUTPAT_ICD10(D720) | Genetic anomalies of leukocytes | 16 | |
| OUTPAT | OUTPAT_ICD10(D811) | Severe combined immunodeficiency [SCID] with low T- and B-cell numbers | 16 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D520) | Dietary folate deficiency anaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 16 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D539) | Nutritional anaemia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 16 | |
| REIMB | REIMB_KELA(120)_ICD10(D808) | Hypogammaglobulinaemia, Other immunodeficiencies with predominantly antibody defects | 16 | |
| DEATH | DEATH_ICD10(D693) | Idiopathic thrombocytopenic purpura | 15 | |
| INPAT | INPAT_ICD10(D560) | Alpha thalassaemia | 15 | |
| INPAT | INPAT_ICD10(D70) | Agranulocytosis | 15 | |
| INPAT | INPAT_ICD10(D840) | Lymphocyte function antigen-1 [LFA-1] defect | 15 | |
| INPAT | INPAT_ICD10(D8982) | Disease caused by deposition of the light chain of the immunoglobulins | 15 | |
| INPAT | INPAT_ICD9(2810A) | Other deficiency anaemias, Pernicious anaemia | 15 | |
| INPAT | INPAT_ICD9(2839X) | Acquired hemolytic anemia, unspecified | 15 | |
| OUTPAT | OUTPAT_ICD10(D69) | Purpura and other haemorrhagic conditions | 15 | |
| OUTPAT | OUTPAT_ICD10(D71) | Functional disorders of polymorphonuclear neutrophils | 15 | |
| OUTPAT | OUTPAT_ICD10(D8413) | Hereditary angioedema type III | 15 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D582) | Other haemoglobinopathies. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 15 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D731) | Hypersplenism. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 15 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D802) | Selective deficiency of immunoglobulin A [IgA]. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 15 | |
| REIMB | REIMB_KELA(120)_ICD10(D809) | Hypogammaglobulinaemia, Immunodeficiency with predominantly antibody defects, unspecified | 15 | |
| REIMB | REIMB_KELA(120)_ICD8(NA) | Hypogammaglobulinaemia, Name not found | 15 | |
| DEATH | DEATH_ICD10(D62) | Acute posthaemorrhagic anaemia | 14 | |
| DEATH | DEATH_ICD10(D696) | Thrombocytopenia, unspecified | 14 | |
| INPAT | INPAT_ICD10(D594) | Other nonautoimmune haemolytic anaemias | 14 | |
| INPAT | INPAT_ICD10(D734) | Cyst of spleen | 14 | |
| INPAT | INPAT_ICD10(D750) | Familial erythrocytosis | 14 | |
| INPAT | INPAT_ICD10(D830) | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function | 14 | |
| INPAT | INPAT_ICD10(D838) | Other common variable immunodeficiencies | 14 | |
| INPAT | INPAT_ICD10(D890) | Polyclonal hypergammaglobulinaemia | 14 | |
| OUTPAT | OUTPAT_ICD10(D5691) | Thalassemia minor | 14 | |
| OUTPAT | OUTPAT_ICD10(D824) | Hyperimmunoglobulin E [IgE] syndrome | 14 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D511) | Vitamin B12deficiency anaemia due to selective vitamin B12malabsorption with proteinuria. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 14 | |
| REIMB | REIMB_KELA(107)_ICD10(C169) | Pernicious anaemia, Stomach, unspecified | 14 | |
| REIMB | REIMB_KELA(107)_ICD9(2810) | Pernicious anaemia, Name not found | 14 | |
| DEATH | DEATH_ICD10(D868) | Sarcoidosis of other and combined sites | 13 | |
| INPAT | INPAT_ICD10(D67) | Hereditary factor IX deficiency | 13 | |
| INPAT | INPAT_ICD10(D7601) | Histiocytosis X (chronic) | 13 | |
| INPAT | INPAT_ICD10(D891) | Cryoglobulinaemia | 13 | |
| INPAT | INPAT_ICD8(28698) | Coagulation defects, Other | 13 | |
| INPAT | INPAT_ICD8(28711) | Purpura and other haemorrhagic conditions, Thrombocytopenia symptomatica | 13 | |
| INPAT | INPAT_ICD9(2820A) | Hereditary spherocytosis | 13 | |
| INPAT | INPAT_ICD9(2830A) | Acquired haemolytic anaemias, Autoimmune haemolytic anaemias | 13 | |
| OUTPAT | OUTPAT_ICD10(D644) | Congenital dyserythropoietic anaemia | 13 | |
| OUTPAT | OUTPAT_ICD10(D67) | Hereditary factor IX deficiency | 13 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D512) | Transcobalamin II deficiency. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 13 | |
| DEATH | DEATH_ICD10(D860) | Sarcoidosis of lung | 12 | |
| DEATH | DEATH_ICD10(D898) | Name not found | 12 | |
| INPAT | INPAT_ICD10(D730) | Hyposplenism | 12 | |
| INPAT | INPAT_ICD10(D733) | Abscess of spleen | 12 | |
| INPAT | INPAT_ICD10(D763) | Other histiocytosis syndromes | 12 | |
| INPAT | INPAT_ICD10(D831) | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders | 12 | |
| INPAT | INPAT_ICD10(D8418) | Other specified defect in the complement system | 12 | |
| INPAT | INPAT_ICD8(28099) | Name not found | 12 | |
| INPAT | INPAT_ICD9(2883X) | Diseases of white blood cells, Eosinophilia | 12 | |
| INPAT | INPAT_ICD9(2888A) | Diseases of white blood cells, Other specified disease of white blood cells | 12 | |
| OUTPAT | OUTPAT_ICD10(D840) | Lymphocyte function antigen-1 [LFA-1] defect | 12 | |
| REIMB | REIMB_KELA(122)_ICD10(D613) | Aplastic anaemia, Idiopathic aplastic anaemia | 12 | |
| REIMB | REIMB_KELA(132)_ICD9(135) | Sarcoidosis, Sarcoidosis | 12 | |
| INPAT | INPAT_ICD10(D51) | Vitamin B12deficiency anaemia | 11 | |
| INPAT | INPAT_ICD10(D578) | Other sickle-cell disorders | 11 | |
| INPAT | INPAT_ICD9(2872B) | Other nonthrombocytopenic purpuras | 11 | |
| OUTPAT | OUTPAT_ICD10(D559) | Anaemia due to enzyme disorder, unspecified | 11 | |
| OUTPAT | OUTPAT_ICD10(D571) | Sickle-cell anaemia without crisis | 11 | |
| OUTPAT | OUTPAT_ICD10(D601) | Transient acquired pure red cell aplasia | 11 | |
| OUTPAT | OUTPAT_ICD10(D804) | Selective deficiency of immunoglobulin M [IgM] | 11 | |
| OUTPAT | OUTPAT_ICD10(D821) | Di George's syndrome | 11 | |
| OUTPAT | OUTPAT_ICD10(D822) | Immunodeficiency with short-limbed stature | 11 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D561) | Beta thalassaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 11 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D580) | Hereditary spherocytosis. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 11 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D800) | Hereditary hypogammaglobulinaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 11 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D8418) | Other specified defect in the complement system. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 11 | |
| REIMB | REIMB_KELA(120)_ICD10(D803) | Hypogammaglobulinaemia, Selective deficiency of immunoglobulin G [IgG] subclasses | 11 | |
| REIMB | REIMB_KELA(120)_ICD10(D83) | Hypogammaglobulinaemia, Common variable immunodeficiency | 11 | |
| DEATH | DEATH_ICD10(D591) | Other autoimmune haemolytic anaemias | 10 | |
| INPAT | INPAT_ICD10(D590) | Drug-induced autoimmune haemolytic anaemia | 10 | |
| INPAT | INPAT_ICD10(D618) | Other specified aplastic anaemias | 10 | |
| INPAT | INPAT_ICD10(D812) | Severe combined immunodeficiency [SCID] with low or normal B-cell numbers | 10 | |
| INPAT | INPAT_ICD10(D841) | Defects in the complement system | 10 | |
| OUTPAT | OUTPAT_ICD10(D511) | Vitamin B12deficiency anaemia due to selective vitamin B12malabsorption with proteinuria | 10 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D619) | Aplastic anaemia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 10 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D694) | Other primary thrombocytopenia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 10 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D89) | Other disorders involving the immune mechanism, not elsewhere classified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 10 | |
| REIMB | REIMB_KELA(120)_ICD10(D839) | Hypogammaglobulinaemia, Common variable immunodeficiency, unspecified | 10 | |
| REIMB | REIMB_KELA(132)_ICD9(1350) | Sarcoidosis, Name not found | 10 | |
| DEATH | DEATH_ICD10(D65) | Disseminated intravascular coagulation [defibrination syndrome] | 9 | |
| INPAT | INPAT_ICD10(D600) | Chronic acquired pure red cell aplasia | 9 | |
| INPAT | INPAT_ICD10(D758) | Other specified diseases of blood and blood-forming organs | 9 | |
| INPAT | INPAT_ICD8(28390) | Acquired haemolytic anaemias, Autoimmunisatoria primaria | 9 | |
| INPAT | INPAT_ICD8(28798) | Purpura and other haemorrhagic conditions, Purpura et status haemorrhagicus alius | 9 | |
| INPAT | INPAT_ICD9(2790A) | Disorders involving the immune mechanism, Deficiency of humoral immunity | 9 | |
| INPAT | INPAT_ICD9(2879X) | Unspecified hemorrhagic conditions | 9 | |
| INPAT | INPAT_ICD9(2898X) | Other specified diseases of blood and blood-forming organs | 9 | |
| OUTPAT | OUTPAT_ICD10(D612) | Aplastic anaemia due to other external agents | 9 | |
| OUTPAT | OUTPAT_ICD10(D642) | Secondary sideroblastic anaemia due to drugs and toxins | 9 | |
| OUTPAT | OUTPAT_ICD10(D8412) | Hereditary angioedema type II | 9 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D528) | Other folate deficiency anaemias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 9 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D538) | Other specified nutritional anaemias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 9 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D82) | Immunodeficiency associated with other major defects. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 9 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D839) | Common variable immunodeficiency, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 9 | |
| REIMB | REIMB_KELA(107)_ICD10(C160) | Pernicious anaemia, Cardia | 9 | |
| REIMB | REIMB_KELA(107)_ICD9(2811A) | Pernicious anaemia, Other vitamin B12 deficiency anemia | 9 | |
| DEATH | DEATH_ICD10(D510) | Vitamin B12deficiency anaemia due to intrinsic factor deficiency | 8 | |
| DEATH | DEATH_ICD10(D70) | Agranulocytosis | 8 | |
| DEATH | DEATH_ICD10(D801) | Nonfamilial hypogammaglobulinaemia | 8 | |
| INPAT | INPAT_ICD10(D513) | Other dietary vitamin B12deficiency anaemia | 8 | |
| INPAT | INPAT_ICD10(D561) | Beta thalassaemia | 8 | |
| INPAT | INPAT_ICD10(D7600) | Eosinophilic granuloma | 8 | |
| INPAT | INPAT_ICD10(D819) | Combined immunodeficiency, unspecified | 8 | |
| INPAT | INPAT_ICD10(D824) | Hyperimmunoglobulin E [IgE] syndrome | 8 | |
| INPAT | INPAT_ICD10(D8411) | Hereditary angioedema type I | 8 | |
| INPAT | INPAT_ICD8(28120) | Other vitamin B12 deficiency anaemia, Folic acid deficiency anaemia | 8 | |
| INPAT | INPAT_ICD8(28500) | Other and unspecified anaemias, Hypochromic anaemia with iron loading | 8 | |
| INPAT | INPAT_ICD9(2890X) | Other diseases of blood and blood-forming organs, Polycythaemia, secondary | 8 | |
| OUTPAT | OUTPAT_ICD10(D512) | Transcobalamin II deficiency | 8 | |
| OUTPAT | OUTPAT_ICD10(D528) | Other folate deficiency anaemias | 8 | |
| OUTPAT | OUTPAT_ICD10(D562) | Delta-beta thalassaemia | 8 | |
| OUTPAT | OUTPAT_ICD10(D581) | Hereditary elliptocytosis | 8 | |
| OUTPAT | OUTPAT_ICD10(D588) | Other specified hereditary haemolytic anaemias | 8 | |
| OUTPAT | OUTPAT_ICD10(D589) | Hereditary haemolytic anaemia, unspecified | 8 | |
| OUTPAT | OUTPAT_ICD10(D708) | Name not found | 8 | |
| OUTPAT | OUTPAT_ICD10(D732) | Chronic congestive splenomegaly | 8 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D758) | Other specified diseases of blood and blood-forming organs. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 8 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D849) | Immunodeficiency, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 8 | |
| REIMB | REIMB_KELA(122)_ICD10(D60) | Aplastic anaemia, Acquired pure red cell aplasia [erythroblastopenia] | 8 | |
| INPAT | INPAT_ICD10(D592) | Drug-induced nonautoimmune haemolytic anaemia | 7 | |
| INPAT | INPAT_ICD10(D601) | Transient acquired pure red cell aplasia | 7 | |
| INPAT | INPAT_ICD10(D64) | Other anaemias | 7 | |
| INPAT | INPAT_ICD10(D720) | Genetic anomalies of leukocytes | 7 | |
| INPAT | INPAT_ICD10(D822) | Immunodeficiency with short-limbed stature | 7 | |
| INPAT | INPAT_ICD10(D828) | Immunodeficiency associated with other specified major defects | 7 | |
| INPAT | INPAT_ICD10(D8419) | Unspecified defect in the complement system | 7 | |
| INPAT | INPAT_ICD10(D848) | Other specified immunodeficiencies | 7 | |
| INPAT | INPAT_ICD8(28398) | Acquired haemolytic anaemias, Aliae definitar | 7 | |
| INPAT | INPAT_ICD9(2873X) | Purpura and other haemorrhagic conditions, Primary thrombocytopenia | 7 | |
| INPAT | INPAT_ICD9(2874X) | Purpura and other haemorrhagic conditions, Secondary thrombocytopenia | 7 | |
| OUTPAT | OUTPAT_ICD10(D75) | Other diseases of blood and blood-forming organs | 7 | |
| OUTPAT | OUTPAT_ICD10(D805) | Immunodeficiency with increased immunoglobulin M [IgM] | 7 | |
| OUTPAT | OUTPAT_ICD10(D828) | Immunodeficiency associated with other specified major defects | 7 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D609) | Acquired pure red cell aplasia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 7 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D610) | Constitutional aplastic anaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 7 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D70) | Agranulocytosis. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 7 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D7081) | Neutropenia congenital. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 7 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D730) | Hyposplenism. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 7 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D848) | Other specified immunodeficiencies. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 7 | |
| REIMB | REIMB_KELA(107)_ICD9(2662A) | Pernicious anaemia, Deficiency of B-complex components, Other B-complex deficiencies | 7 | |
| REIMB | REIMB_KELA(120)_ICD10(D830) | Hypogammaglobulinaemia, Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function | 7 | |
| REIMB | REIMB_KELA(120)_ICD9(NA) | Hypogammaglobulinaemia, Name not found | 7 | |
| REIMB | REIMB_KELA(132)_ICD10(NA) | Sarcoidosis, Name not found | 7 | |
| DEATH | DEATH_ICD10(D599) | Acquired haemolytic anaemia, unspecified | 6 | |
| DEATH | DEATH_ICD10(D761) | Haemophagocytic lymphohistiocytosis | 6 | |
| INPAT | INPAT_ICD10(D5699) | Thalassaemia, unspecified | 6 | |
| INPAT | INPAT_ICD10(D570) | Sickle-cell anaemia with crisis | 6 | |
| INPAT | INPAT_ICD10(D589) | Hereditary haemolytic anaemia, unspecified | 6 | |
| INPAT | INPAT_ICD10(D595) | Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli] | 6 | |
| INPAT | INPAT_ICD10(D642) | Secondary sideroblastic anaemia due to drugs and toxins | 6 | |
| INPAT | INPAT_ICD10(D811) | Severe combined immunodeficiency [SCID] with low T- and B-cell numbers | 6 | |
| INPAT | INPAT_ICD10(D813) | Adenosine deaminase [ADA] deficiency | 6 | |
| INPAT | INPAT_ICD10(D8413) | Hereditary angioedema type III | 6 | |
| INPAT | INPAT_ICD8(28402) | Aplastic anaemia, Acquisita secundaria | 6 | |
| INPAT | INPAT_ICD9(2830X) | Acquired haemolytic anaemias, Autoimmune haemolytic anaemias | 6 | |
| INPAT | INPAT_ICD9(2869X) | Other and unspecified coagulation defects | 6 | |
| OUTPAT | OUTPAT_ICD10(D550) | Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency | 6 | |
| OUTPAT | OUTPAT_ICD10(D570) | Sickle-cell anaemia with crisis | 6 | |
| OUTPAT | OUTPAT_ICD10(D592) | Drug-induced nonautoimmune haemolytic anaemia | 6 | |
| OUTPAT | OUTPAT_ICD10(D608) | Other acquired pure red cell aplasias | 6 | |
| OUTPAT | OUTPAT_ICD10(D681) | Hereditary factor XI deficiency | 6 | |
| OUTPAT | OUTPAT_ICD10(D749) | Methaemoglobinaemia, unspecified | 6 | |
| OUTPAT | OUTPAT_ICD10(D812) | Severe combined immunodeficiency [SCID] with low or normal B-cell numbers | 6 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D56) | Thalassaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 6 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D560) | Alpha thalassaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 6 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D891) | Cryoglobulinaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 6 | |
| DEATH | DEATH_ICD10(D619) | Aplastic anaemia, unspecified | 5 | |
| DEATH | DEATH_ICD10(D695) | Secondary thrombocytopenia | 5 | |
| DEATH | DEATH_ICD10(D752) | Essential thrombocytosis | 5 | |
| INPAT | INPAT_ICD10(D511) | Vitamin B12deficiency anaemia due to selective vitamin B12malabsorption with proteinuria | 5 | |
| INPAT | INPAT_ICD10(D521) | Drug-induced folate deficiency anaemia | 5 | |
| INPAT | INPAT_ICD10(D71) | Functional disorders of polymorphonuclear neutrophils | 5 | |
| INPAT | INPAT_ICD10(D821) | Di George's syndrome | 5 | |
| INPAT | INPAT_ICD10(D892) | Hypergammaglobulinaemia, unspecified | 5 | |
| INPAT | INPAT_ICD8(13500) | Name not found | 5 | |
| INPAT | INPAT_ICD8(28299) | Hereditary haemolytic anaemias, Other | 5 | |
| INPAT | INPAT_ICD8(28300) | Acquired haemolytic anaemias, Acute | 5 | |
| INPAT | INPAT_ICD8(28391) | Acquired haemolytic anaemias, Autoimmunisatoria secundaria | 5 | |
| INPAT | INPAT_ICD8(28409) | Aplastic anaemia, Unspecified | 5 | |
| INPAT | INPAT_ICD8(28588) | Other and unspecified anaemias, Other specified anaemia | 5 | |
| INPAT | INPAT_ICD8(28610) | Coagulation defects, Christmas disease | 5 | |
| INPAT | INPAT_ICD8(28730) | Purpura and other haemorrhagic conditions, Thrombocytopathy | 5 | |
| INPAT | INPAT_ICD9(2798X) | Disorders involving the immune mechanism, Other specified disorders involving the immune mechanism | 5 | |
| INPAT | INPAT_ICD9(2848X) | Aplastic anaemia, Other specified aplastic anaemias | 5 | |
| INPAT | INPAT_ICD9(2870X) | Purpura and other haemorrhagic conditions, Allergic purpura | 5 | |
| INPAT | INPAT_ICD9(2873C) | Purpura and other haemorrhagic conditions, Primary thrombocytopenia | 5 | |
| INPAT | INPAT_ICD9(2878X) | Other specified hemorrhagic conditions | 5 | |
| INPAT | INPAT_ICD9(2890A) | Other diseases of blood and blood-forming organs, Polycythaemia, secondary | 5 | |
| INPAT | INPAT_ICD9(2899X) | Unspecified diseases of blood and blood-forming organs | 5 | |
| OUTPAT | OUTPAT_ICD10(D538) | Other specified nutritional anaemias | 5 | |
| OUTPAT | OUTPAT_ICD10(D596) | Haemoglobinuria due to haemolysis from other external causes | 5 | |
| OUTPAT | OUTPAT_ICD10(D733) | Abscess of spleen | 5 | |
| OUTPAT | OUTPAT_ICD10(D829) | Immunodeficiency associated with major defect, unspecified | 5 | |
| OUTPAT | OUTPAT_ICD10(D8414) | C1 esterase inhibitor deficiency (C1-INH deficiency) | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D501) | Sideropenic dysphagia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D5691) | Thalassemia minor. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D5699) | Thalassaemia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D613) | Idiopathic aplastic anaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D684) | Acquired coagulation factor deficiency. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D735) | Infarction of spleen. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D739) | Disease of spleen, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D763) | Other histiocytosis syndromes. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D824) | Hyperimmunoglobulin E [IgE] syndrome. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D84) | Other immunodeficiencies. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D841) | Defects in the complement system. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D8411) | Hereditary angioedema type I. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D8989) | Other specified disorders involving the immune mechanism, not elsewhere classified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| REIMB | REIMB_KELA(107)_ICD10(D513) | Pernicious anaemia, Other dietary vitamin B12deficiency anaemia | 5 | |
| REIMB | REIMB_KELA(107)_ICD9(266) | Pernicious anaemia, Deficiency of B-complex components | 5 | |
| REIMB | REIMB_KELA(107)_ICD9(2811) | Pernicious anaemia, Name not found | 5 | |
| REIMB | REIMB_KELA(107)_ICD9(D51) | Pernicious anaemia, Name not found | 5 | |
| REIMB | REIMB_KELA(132)_ICD10(D869) | Sarcoidosis, Sarcoidosis, unspecified | 5 |