Source |
Code |
Name |
Case count |
Share of cases (%) |
OUTPAT |
OUTPAT_ICD10(D649) |
Anaemia, unspecified |
14983 |
|
OUTPAT |
OUTPAT_ICD10(D509) |
Iron deficiency anaemia, unspecified |
11000 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D649) |
Anaemia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
8796 |
|
INPAT |
INPAT_ICD10(D649) |
Anaemia, unspecified |
8549 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D509) |
Iron deficiency anaemia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
6009 |
|
INPAT |
INPAT_ICD10(D509) |
Iron deficiency anaemia, unspecified |
5434 |
|
OUTPAT |
OUTPAT_ICD10(D500) |
Iron deficiency anaemia secondary to blood loss (chronic) |
3748 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D50) |
Iron deficiency anaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
3550 |
|
INPAT |
INPAT_ICD10(D500) |
Iron deficiency anaemia secondary to blood loss (chronic) |
2831 |
|
INPAT |
INPAT_ICD10(D7082) |
Drug-induced neutropenia |
2171 |
|
OUTPAT |
OUTPAT_ICD10(D696) |
Thrombocytopenia, unspecified |
2061 |
|
OUTPAT |
OUTPAT_ICD10(D860) |
Sarcoidosis of lung |
1876 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D500) |
Iron deficiency anaemia secondary to blood loss (chronic). Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
1579 |
|
OUTPAT |
OUTPAT_ICD10(D7089) |
Neutropenic splenomegaly |
1481 |
|
OUTPAT |
OUTPAT_ICD10(D7082) |
Drug-induced neutropenia |
1459 |
|
OUTPAT |
OUTPAT_ICD10(D868) |
Sarcoidosis of other and combined sites |
1408 |
|
OUTPAT |
OUTPAT_ICD10(D862) |
Sarcoidosis of lung with sarcoidosis of lymph nodes |
1390 |
|
OUTPAT |
OUTPAT_ICD10(D688) |
Other specified coagulation defects |
1367 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D648) |
Other specified anaemias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
1324 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D508) |
Other iron deficiency anaemias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
1296 |
|
INPAT |
INPAT_ICD8(28920) |
Other disease of blood and blood-forming organs, Nonspecific mesenteric lymphadenitis |
1290 |
|
INPAT |
INPAT_ICD10(D696) |
Thrombocytopenia, unspecified |
1134 |
|
OUTPAT |
OUTPAT_ICD10(D508) |
Other iron deficiency anaemias |
1115 |
|
OUTPAT |
OUTPAT_ICD10(D869) |
Sarcoidosis, unspecified |
1078 |
|
OUTPAT |
OUTPAT_ICD10(D728) |
Other specified disorders of white blood cells |
1076 |
|
OUTPAT |
OUTPAT_ICD10(D648) |
Other specified anaemias |
1066 |
|
OUTPAT |
OUTPAT_ICD10(D693) |
Idiopathic thrombocytopenic purpura |
928 |
|
OUTPAT |
OUTPAT_ICD10(D861) |
Sarcoidosis of lymph nodes |
900 |
|
INPAT |
INPAT_ICD10(D62) |
Acute posthaemorrhagic anaemia |
872 |
|
OUTPAT |
OUTPAT_ICD10(D752) |
Essential thrombocytosis |
871 |
|
OUTPAT |
OUTPAT_ICD10(D690) |
Allergic purpura |
859 |
|
INPAT |
INPAT_ICD10(D7089) |
Neutropenic splenomegaly |
834 |
|
OUTPAT |
OUTPAT_ICD10(D8980) |
Immunoglobulin A (IgA) deposits in organisms |
831 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D519) |
Vitamin B12deficiency anaemia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
806 |
|
OUTPAT |
OUTPAT_ICD10(D751) |
Secondary polycythaemia |
741 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D696) |
Thrombocytopenia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
714 |
|
INPAT |
INPAT_ICD8(28000) |
Iron deficiency anaemias, Posthaemorrhagica |
713 |
|
OUTPAT |
OUTPAT_ICD10(D519) |
Vitamin B12deficiency anaemia, unspecified |
710 |
|
OUTPAT |
OUTPAT_ICD10(D759) |
Disease of blood and blood-forming organs, unspecified |
658 |
|
OUTPAT |
OUTPAT_ICD10(D62) |
Acute posthaemorrhagic anaemia |
626 |
|
INPAT |
INPAT_ICD10(D688) |
Other specified coagulation defects |
599 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D51) |
Vitamin B12deficiency anaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
596 |
|
INPAT |
INPAT_ICD10(D648) |
Other specified anaemias |
591 |
|
INPAT |
INPAT_ICD10(D693) |
Idiopathic thrombocytopenic purpura |
571 |
|
INPAT |
INPAT_ICD10(D860) |
Sarcoidosis of lung |
569 |
|
INPAT |
INPAT_ICD10(D868) |
Sarcoidosis of other and combined sites |
560 |
|
OUTPAT |
OUTPAT_ICD10(D638) |
Anaemia in other chronic diseases classified elsewhere |
560 |
|
INPAT |
INPAT_ICD10(D519) |
Vitamin B12deficiency anaemia, unspecified |
548 |
|
OUTPAT |
OUTPAT_ICD10(D50) |
Iron deficiency anaemia |
544 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D688) |
Other specified coagulation defects. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
543 |
|
OUTPAT |
OUTPAT_ICD10(D510) |
Vitamin B12deficiency anaemia due to intrinsic factor deficiency |
508 |
|
OUTPAT |
OUTPAT_ICD10(D721) |
Eosinophilia |
489 |
|
INPAT |
INPAT_ICD10(D8980) |
Immunoglobulin A (IgA) deposits in organisms |
488 |
|
INPAT |
INPAT_ICD8(28009) |
Iron deficiency anaemias, Unspecified |
483 |
|
OUTPAT |
OUTPAT_ICD10(D680) |
Von Willebrand's disease |
439 |
|
OUTPAT |
OUTPAT_ICD10(D699) |
Haemorrhagic condition, unspecified |
420 |
|
INPAT |
INPAT_ICD9(2800A) |
Iron deficiency anemia secondary to blood loss (chronic) |
409 |
|
OUTPAT |
OUTPAT_ICD10(D689) |
Coagulation defect, unspecified |
396 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D752) |
Essential thrombocytosis. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
377 |
|
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! |
374 |
|
OUTPAT |
OUTPAT_ICD10(D863) |
Sarcoidosis of skin |
367 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D860) |
Sarcoidosis of lung. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
361 |
|
OUTPAT |
OUTPAT_ICD10(D801) |
Nonfamilial hypogammaglobulinaemia |
360 |
|
INPAT |
INPAT_ICD10(D508) |
Other iron deficiency anaemias |
355 |
|
OUTPAT |
OUTPAT_ICD10(D591) |
Other autoimmune haemolytic anaemias |
332 |
|
INPAT |
INPAT_ICD9(2809X) |
Iron deficiency anemia, unspecified |
330 |
|
INPAT |
INPAT_ICD10(D869) |
Sarcoidosis, unspecified |
324 |
|
INPAT |
INPAT_ICD10(D690) |
Allergic purpura |
320 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D64) |
Other anaemias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
318 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D8980) |
Immunoglobulin A (IgA) deposits in organisms. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
313 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D868) |
Sarcoidosis of other and combined sites. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
312 |
|
INPAT |
INPAT_ICD10(D638) |
Anaemia in other chronic diseases classified elsewhere |
303 |
|
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! |
290 |
|
INPAT |
INPAT_ICD10(D862) |
Sarcoidosis of lung with sarcoidosis of lymph nodes |
286 |
|
OUTPAT |
OUTPAT_ICD10(D682) |
Hereditary deficiency of other clotting factors |
286 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D62) |
Acute posthaemorrhagic anaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
285 |
|
INPAT |
INPAT_ICD10(D510) |
Vitamin B12deficiency anaemia due to intrinsic factor deficiency |
281 |
|
INPAT |
INPAT_ICD9(2859X) |
Other and unspecified anaemias, Anaemia, unspecified |
275 |
|
OUTPAT |
OUTPAT_ICD10(D692) |
Other nonthrombocytopenic purpura |
271 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D7089) |
Neutropenic splenomegaly. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
266 |
|
INPAT |
INPAT_ICD10(D695) |
Secondary thrombocytopenia |
263 |
|
INPAT |
INPAT_ICD10(D680) |
Von Willebrand's disease |
260 |
|
OUTPAT |
OUTPAT_ICD10(D809) |
Immunodeficiency with predominantly antibody defects, unspecified |
260 |
|
INPAT |
INPAT_ICD10(D591) |
Other autoimmune haemolytic anaemias |
259 |
|
OUTPAT |
OUTPAT_ICD10(D729) |
Disorder of white blood cells, unspecified |
248 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D690) |
Allergic purpura. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
242 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D86) |
Sarcoidosis. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
236 |
|
OUTPAT |
OUTPAT_ICD10(D803) |
Selective deficiency of immunoglobulin G [IgG] subclasses |
231 |
|
INPAT |
INPAT_ICD10(D752) |
Essential thrombocytosis |
224 |
|
OUTPAT |
OUTPAT_ICD10(D695) |
Secondary thrombocytopenia |
220 |
|
INPAT |
INPAT_ICD8(28930) |
Other disease of blood and blood-forming organs, Lymphadenitis, unspecified, except mesenteric |
215 |
|
DEATH |
DEATH_ICD10(D683) |
Haemorrhagic disorder due to circulating anticoagulants |
214 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D693) |
Idiopathic thrombocytopenic purpura. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
201 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D699) |
Haemorrhagic condition, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
201 |
|
OUTPAT |
OUTPAT_ICD10(D808) |
Other immunodeficiencies with predominantly antibody defects |
198 |
|
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! |
197 |
|
OUTPAT |
OUTPAT_ICD10(D599) |
Acquired haemolytic anaemia, unspecified |
191 |
|
INPAT |
INPAT_ICD8(28008) |
Iron deficiency anaemias, Alia definita |
189 |
|
INPAT |
INPAT_ICD10(D728) |
Other specified disorders of white blood cells |
185 |
|
INPAT |
INPAT_ICD10(D721) |
Eosinophilia |
182 |
|
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! |
179 |
|
INPAT |
INPAT_ICD10(D861) |
Sarcoidosis of lymph nodes |
173 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D518) |
Other vitamin B12deficiency anaemias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
173 |
|
OUTPAT |
OUTPAT_ICD10(D750) |
Familial erythrocytosis |
169 |
|
OUTPAT |
OUTPAT_ICD10(D531) |
Other megaloblastic anaemias, not elsewhere classified |
166 |
|
INPAT |
INPAT_ICD10(D801) |
Nonfamilial hypogammaglobulinaemia |
164 |
|
INPAT |
INPAT_ICD8(28700) |
Purpura and other haemorrhagic conditions, Allergic purpura |
163 |
|
INPAT |
INPAT_ICD10(D735) |
Infarction of spleen |
158 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D751) |
Secondary polycythaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
155 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D69) |
Purpura and other haemorrhagic conditions. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
153 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D698) |
Other specified haemorrhagic conditions. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
149 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D729) |
Disorder of white blood cells, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
147 |
|
OUTPAT |
OUTPAT_ICD10(D683) |
Haemorrhagic disorder due to circulating anticoagulants |
144 |
|
INPAT |
INPAT_ICD10(D682) |
Hereditary deficiency of other clotting factors |
140 |
|
OUTPAT |
OUTPAT_ICD10(D619) |
Aplastic anaemia, unspecified |
139 |
|
OUTPAT |
OUTPAT_ICD10(D518) |
Other vitamin B12deficiency anaemias |
135 |
|
INPAT |
INPAT_ICD10(D50) |
Iron deficiency anaemia |
130 |
|
INPAT |
INPAT_ICD9(2873A) |
Purpura and other haemorrhagic conditions, Primary thrombocytopenia |
128 |
|
INPAT |
INPAT_ICD10(D699) |
Haemorrhagic condition, unspecified |
127 |
|
INPAT |
INPAT_ICD8(28719) |
Purpura and other haemorrhagic conditions, Thrombocytopenia NUD |
127 |
|
OUTPAT |
OUTPAT_ICD10(D802) |
Selective deficiency of immunoglobulin A [IgA] |
126 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D680) |
Von Willebrand's disease. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
126 |
|
OUTPAT |
OUTPAT_ICD10(D8989) |
Other specified disorders involving the immune mechanism, not elsewhere classified |
124 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D869) |
Sarcoidosis, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
123 |
|
OUTPAT |
OUTPAT_ICD10(D735) |
Infarction of spleen |
122 |
|
OUTPAT |
OUTPAT_ICD10(D731) |
Hypersplenism |
121 |
|
OUTPAT |
OUTPAT_ICD10(D698) |
Other specified haemorrhagic conditions |
120 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D689) |
Coagulation defect, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
120 |
|
INPAT |
INPAT_ICD10(D599) |
Acquired haemolytic anaemia, unspecified |
119 |
|
INPAT |
INPAT_ICD9(2851A) |
Acute posthemorrhagic anemia |
117 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D529) |
Folate deficiency anaemia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
117 |
|
INPAT |
INPAT_ICD10(D531) |
Other megaloblastic anaemias, not elsewhere classified |
116 |
|
OUTPAT |
OUTPAT_ICD10(D691) |
Qualitative platelet defects |
115 |
|
INPAT |
INPAT_ICD10(D630) |
Anaemia in neoplastic disease (C00-D48+) |
114 |
|
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! |
113 |
|
OUTPAT |
OUTPAT_ICD10(D8418) |
Other specified defect in the complement system |
112 |
|
INPAT |
INPAT_ICD8(28910) |
Other disease of blood and blood-forming organs, Chronic lymphadenitis |
111 |
|
OUTPAT |
OUTPAT_ICD10(D800) |
Hereditary hypogammaglobulinaemia |
110 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D7082) |
Drug-induced neutropenia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
108 |
|
OUTPAT |
OUTPAT_ICD10(D758) |
Other specified diseases of blood and blood-forming organs |
106 |
|
INPAT |
INPAT_ICD10(D529) |
Folate deficiency anaemia, unspecified |
105 |
|
DEATH |
DEATH_ICD10(D649) |
Anaemia, unspecified |
103 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D531) |
Other megaloblastic anaemias, not elsewhere classified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
101 |
|
INPAT |
INPAT_ICD10(D683) |
Haemorrhagic disorder due to circulating anticoagulants |
99 |
|
OUTPAT |
OUTPAT_ICD10(D694) |
Other primary thrombocytopenia |
99 |
|
INPAT |
INPAT_ICD10(D689) |
Coagulation defect, unspecified |
98 |
|
INPAT |
INPAT_ICD9(2870A) |
Purpura and other haemorrhagic conditions, Allergic purpura |
98 |
|
OUTPAT |
OUTPAT_ICD10(D529) |
Folate deficiency anaemia, unspecified |
98 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D692) |
Other nonthrombocytopenic purpura. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
97 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D682) |
Hereditary deficiency of other clotting factors. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
93 |
|
INPAT |
INPAT_ICD10(D619) |
Aplastic anaemia, unspecified |
91 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D861) |
Sarcoidosis of lymph nodes. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
90 |
|
INPAT |
INPAT_ICD10(D809) |
Immunodeficiency with predominantly antibody defects, unspecified |
89 |
|
OUTPAT |
OUTPAT_ICD10(D814) |
Nezelof's syndrome |
89 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D721) |
Eosinophilia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
89 |
|
INPAT |
INPAT_ICD10(D759) |
Disease of blood and blood-forming organs, unspecified |
87 |
|
OUTPAT |
OUTPAT_ICD10(D839) |
Common variable immunodeficiency, unspecified |
86 |
|
INPAT |
INPAT_ICD10(D810) |
Severe combined immunodeficiency [SCID] with reticular dysgenesis |
84 |
|
INPAT |
INPAT_ICD10(D751) |
Secondary polycythaemia |
82 |
|
OUTPAT |
OUTPAT_ICD10(D849) |
Immunodeficiency, unspecified |
82 |
|
INPAT |
INPAT_ICD8(28599) |
Other and unspecified anaemias, Anaemia, unspecified |
81 |
|
OUTPAT |
OUTPAT_ICD10(D66) |
Hereditary factor VIII deficiency |
80 |
|
INPAT |
INPAT_ICD10(D65) |
Disseminated intravascular coagulation [defibrination syndrome] |
78 |
|
INPAT |
INPAT_ICD10(D803) |
Selective deficiency of immunoglobulin G [IgG] subclasses |
78 |
|
INPAT |
INPAT_ICD9(2810X) |
Other deficiency anaemias, Pernicious anaemia |
78 |
|
INPAT |
INPAT_ICD9(2888B) |
Diseases of white blood cells, Other specified disease of white blood cells |
78 |
|
OUTPAT |
OUTPAT_ICD10(D501) |
Sideropenic dysphagia |
77 |
|
OUTPAT |
OUTPAT_ICD10(D643) |
Other sideroblastic anaemias |
77 |
|
OUTPAT |
OUTPAT_ICD10(D899) |
Disorder involving the immune mechanism, unspecified |
76 |
|
OUTPAT |
OUTPAT_ICD10(D830) |
Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function |
75 |
|
OUTPAT |
OUTPAT_ICD10(D640) |
Hereditary sideroblastic anaemia |
74 |
|
OUTPAT |
OUTPAT_ICD10(D593) |
Haemolytic-uraemic syndrome |
73 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D591) |
Other autoimmune haemolytic anaemias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
73 |
|
INPAT |
INPAT_ICD10(D814) |
Nezelof's syndrome |
72 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D801) |
Nonfamilial hypogammaglobulinaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
71 |
|
OUTPAT |
OUTPAT_ICD10(D609) |
Acquired pure red cell aplasia, unspecified |
69 |
|
INPAT |
INPAT_ICD10(D640) |
Hereditary sideroblastic anaemia |
68 |
|
OUTPAT |
OUTPAT_ICD10(D630) |
Anaemia in neoplastic disease (C00-D48+) |
68 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D52) |
Folate deficiency anaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
67 |
|
OUTPAT |
OUTPAT_ICD10(D841) |
Defects in the complement system |
65 |
|
OUTPAT |
OUTPAT_ICD10(D580) |
Hereditary spherocytosis |
63 |
|
OUTPAT |
OUTPAT_ICD10(D582) |
Other haemoglobinopathies |
63 |
|
OUTPAT |
OUTPAT_ICD10(D739) |
Disease of spleen, unspecified |
63 |
|
INPAT |
INPAT_ICD10(D808) |
Other immunodeficiencies with predominantly antibody defects |
62 |
|
INPAT |
INPAT_ICD10(D731) |
Hypersplenism |
60 |
|
OUTPAT |
OUTPAT_ICD10(D734) |
Cyst of spleen |
59 |
|
INPAT |
INPAT_ICD10(D8989) |
Other specified disorders involving the immune mechanism, not elsewhere classified |
58 |
|
INPAT |
INPAT_ICD8(28590) |
Other and unspecified anaemias, Secundaria (e nephropatia, collagenosa, infectione etc.) |
57 |
|
OUTPAT |
OUTPAT_ICD10(D7081) |
Neutropenia congenital |
57 |
|
OUTPAT |
OUTPAT_ICD10(D8419) |
Unspecified defect in the complement system |
57 |
|
INPAT |
INPAT_ICD8(28899) |
Agranulocytosis |
56 |
|
OUTPAT |
OUTPAT_ICD10(D7080) |
Agranulocytic angina |
56 |
|
OUTPAT |
OUTPAT_ICD10(D65) |
Disseminated intravascular coagulation [defibrination syndrome] |
55 |
|
INPAT |
INPAT_ICD9(2808X) |
Other specified iron deficiency anemias |
54 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D68) |
Other coagulation defects. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
54 |
|
INPAT |
INPAT_ICD10(D518) |
Other vitamin B12deficiency anaemias |
53 |
|
INPAT |
INPAT_ICD10(D66) |
Hereditary factor VIII deficiency |
53 |
|
INPAT |
INPAT_ICD8(28799) |
Purpura and other haemorrhagic conditions, Other and unspecified |
53 |
|
INPAT |
INPAT_ICD9(2859A) |
Other and unspecified anaemias, Anaemia, unspecified |
53 |
|
INPAT |
INPAT_ICD10(D643) |
Other sideroblastic anaemias |
52 |
|
INPAT |
INPAT_ICD10(D593) |
Haemolytic-uraemic syndrome |
51 |
|
INPAT |
INPAT_ICD10(D729) |
Disorder of white blood cells, unspecified |
51 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D863) |
Sarcoidosis of skin. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
51 |
|
INPAT |
INPAT_ICD9(2875A) |
Thrombocytopenia, unspecified |
48 |
|
OUTPAT |
OUTPAT_ICD10(D610) |
Constitutional aplastic anaemia |
48 |
|
OUTPAT |
OUTPAT_ICD10(D613) |
Idiopathic aplastic anaemia |
48 |
|
OUTPAT |
OUTPAT_ICD10(D641) |
Secondary sideroblastic anaemia due to disease |
48 |
|
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! |
48 |
|
INPAT |
INPAT_ICD10(D694) |
Other primary thrombocytopenia |
47 |
|
INPAT |
INPAT_ICD8(28900) |
Other disease of blood and blood-forming organs, Polycythaemia, secondary |
46 |
|
INPAT |
INPAT_ICD9(2892A) |
Nonspecific mesenteric lymphadenitis |
46 |
|
OUTPAT |
OUTPAT_ICD10(D684) |
Acquired coagulation factor deficiency |
46 |
|
OUTPAT |
OUTPAT_ICD10(D51) |
Vitamin B12deficiency anaemia |
45 |
|
OUTPAT |
OUTPAT_ICD10(D730) |
Hyposplenism |
45 |
|
INPAT |
INPAT_ICD10(D520) |
Dietary folate deficiency anaemia |
44 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D750) |
Familial erythrocytosis. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
44 |
|
INPAT |
INPAT_ICD10(D692) |
Other nonthrombocytopenic purpura |
43 |
|
OUTPAT |
OUTPAT_ICD10(D891) |
Cryoglobulinaemia |
43 |
|
INPAT |
INPAT_ICD9(2801A) |
Iron deficiency anemia secondary to inadequate dietary iron intake |
42 |
|
OUTPAT |
OUTPAT_ICD10(D594) |
Other nonautoimmune haemolytic anaemias |
42 |
|
OUTPAT |
OUTPAT_ICD10(D69) |
Purpura and other haemorrhagic conditions |
42 |
|
OUTPAT |
OUTPAT_ICD10(D763) |
Other histiocytosis syndromes |
42 |
|
OUTPAT |
OUTPAT_ICD10(D86) |
Sarcoidosis |
42 |
|
OUTPAT |
OUTPAT_ICD10(D539) |
Nutritional anaemia, unspecified |
41 |
|
OUTPAT |
OUTPAT_ICD10(D738) |
Other diseases of spleen |
41 |
|
OUTPAT |
OUTPAT_ICD10(D806) |
Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia |
41 |
|
OUTPAT |
OUTPAT_ICD10(D898) |
Name not found |
41 |
|
INPAT |
INPAT_ICD10(D761) |
Haemophagocytic lymphohistiocytosis |
40 |
|
INPAT |
INPAT_ICD10(D802) |
Selective deficiency of immunoglobulin A [IgA] |
40 |
|
OUTPAT |
OUTPAT_ICD10(D810) |
Severe combined immunodeficiency [SCID] with reticular dysgenesis |
40 |
|
INPAT |
INPAT_ICD10(D839) |
Common variable immunodeficiency, unspecified |
39 |
|
INPAT |
INPAT_ICD9(2849X) |
Aplastic anemia, unspecified |
39 |
|
OUTPAT |
OUTPAT_ICD10(D8982) |
Disease caused by deposition of the light chain of the immunoglobulins |
39 |
|
DEATH |
DEATH_ICD10(D509) |
Iron deficiency anaemia, unspecified |
38 |
|
INPAT |
INPAT_ICD10(D698) |
Other specified haemorrhagic conditions |
38 |
|
INPAT |
INPAT_ICD10(D739) |
Disease of spleen, unspecified |
38 |
|
INPAT |
INPAT_ICD9(2864A) |
Von Willebrand's disease |
38 |
|
INPAT |
INPAT_ICD9(2891A) |
Chronic lymphadenitis |
38 |
|
OUTPAT |
OUTPAT_ICD10(D598) |
Other acquired haemolytic anaemias |
38 |
|
OUTPAT |
OUTPAT_ICD10(D848) |
Other specified immunodeficiencies |
38 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D582) |
Other haemoglobinopathies. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
38 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D599) |
Acquired haemolytic anaemia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
38 |
|
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! |
38 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D809) |
Immunodeficiency with predominantly antibody defects, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
38 |
|
INPAT |
INPAT_ICD8(28998) |
Other disease of blood and blood-forming organs, Alii definiti |
37 |
|
INPAT |
INPAT_ICD10(D613) |
Idiopathic aplastic anaemia |
36 |
|
INPAT |
INPAT_ICD10(D641) |
Secondary sideroblastic anaemia due to disease |
36 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D695) |
Secondary thrombocytopenia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
36 |
|
DEATH |
DEATH_ICD10(D500) |
Iron deficiency anaemia secondary to blood loss (chronic) |
35 |
|
INPAT |
INPAT_ICD10(D863) |
Sarcoidosis of skin |
35 |
|
INPAT |
INPAT_ICD8(28710) |
Purpura and other haemorrhagic conditions, Thrombocytopenia essentialis (Morbus Werlhof) |
35 |
|
OUTPAT |
OUTPAT_ICD10(D563) |
Thalassaemia trait |
35 |
|
OUTPAT |
OUTPAT_ICD10(D64) |
Other anaemias |
35 |
|
OUTPAT |
OUTPAT_ICD10(D8411) |
Hereditary angioedema type I |
35 |
|
INPAT |
INPAT_ICD10(D609) |
Acquired pure red cell aplasia, unspecified |
34 |
|
INPAT |
INPAT_ICD10(D611) |
Drug-induced aplastic anaemia |
34 |
|
INPAT |
INPAT_ICD10(D691) |
Qualitative platelet defects |
34 |
|
OUTPAT |
OUTPAT_ICD10(D838) |
Other common variable immunodeficiencies |
34 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D520) |
Dietary folate deficiency anaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
34 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D802) |
Selective deficiency of immunoglobulin A [IgA]. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
34 |
|
INPAT |
INPAT_ICD10(D580) |
Hereditary spherocytosis |
33 |
|
INPAT |
INPAT_ICD8(28199) |
Other vitamin B12 deficiency anaemia, Other and unspecified deficiency anaemia |
33 |
|
INPAT |
INPAT_ICD8(28200) |
Hereditary haemolytic anaemias, Familial acholuric jaundice |
33 |
|
INPAT |
INPAT_ICD8(28999) |
Other disease of blood and blood-forming organs, Other and unspecified |
33 |
|
OUTPAT |
OUTPAT_ICD10(D520) |
Dietary folate deficiency anaemia |
33 |
|
OUTPAT |
OUTPAT_ICD10(D761) |
Haemophagocytic lymphohistiocytosis |
33 |
|
OUTPAT |
OUTPAT_ICD10(D831) |
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders |
33 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D513) |
Other dietary vitamin B12deficiency anaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
33 |
|
INPAT |
INPAT_ICD10(D501) |
Sideropenic dysphagia |
32 |
|
INPAT |
INPAT_ICD8(28109) |
Other anaemia, Perniciosa non definita |
32 |
|
OUTPAT |
OUTPAT_ICD10(D560) |
Alpha thalassaemia |
32 |
|
OUTPAT |
OUTPAT_ICD10(D70) |
Agranulocytosis |
32 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D643) |
Other sideroblastic anaemias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
32 |
|
INPAT |
INPAT_ICD10(D7081) |
Neutropenia congenital |
31 |
|
INPAT |
INPAT_ICD8(28110) |
Other vitamin B12 deficiency anaemia, Other vitamin B12 deficiency |
31 |
|
OUTPAT |
OUTPAT_ICD10(D7600) |
Eosinophilic granuloma |
31 |
|
OUTPAT |
OUTPAT_ICD10(D892) |
Hypergammaglobulinaemia, unspecified |
31 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D539) |
Nutritional anaemia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
31 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D72) |
Other disorders of white blood cells. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
31 |
|
INPAT |
INPAT_ICD10(D800) |
Hereditary hypogammaglobulinaemia |
30 |
|
OUTPAT |
OUTPAT_ICD10(D611) |
Drug-induced aplastic anaemia |
30 |
|
OUTPAT |
OUTPAT_ICD10(D818) |
Other combined immunodeficiencies |
30 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D683) |
Haemorrhagic disorder due to circulating anticoagulants. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
30 |
|
INPAT |
INPAT_ICD8(28630) |
Coagulation defects, Vascular haemophilia |
29 |
|
INPAT |
INPAT_ICD9(2880B) |
Diseases of white blood cells, Agranulocytosis |
29 |
|
OUTPAT |
OUTPAT_ICD10(D573) |
Sickle-cell trait |
29 |
|
OUTPAT |
OUTPAT_ICD10(D590) |
Drug-induced autoimmune haemolytic anaemia |
29 |
|
OUTPAT |
OUTPAT_ICD10(D819) |
Combined immunodeficiency, unspecified |
29 |
|
DEATH |
DEATH_ICD10(D898) |
Name not found |
28 |
|
INPAT |
INPAT_ICD10(D849) |
Immunodeficiency, unspecified |
28 |
|
OUTPAT |
OUTPAT_ICD10(D8413) |
Hereditary angioedema type III |
28 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D808) |
Other immunodeficiencies with predominantly antibody defects. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
28 |
|
DEATH |
DEATH_ICD10(D868) |
Sarcoidosis of other and combined sites |
27 |
|
INPAT |
INPAT_ICD10(D610) |
Constitutional aplastic anaemia |
27 |
|
INPAT |
INPAT_ICD10(D7080) |
Agranulocytic angina |
27 |
|
INPAT |
INPAT_ICD10(D830) |
Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function |
27 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D691) |
Qualitative platelet defects. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
27 |
|
INPAT |
INPAT_ICD10(D539) |
Nutritional anaemia, unspecified |
26 |
|
INPAT |
INPAT_ICD10(D684) |
Acquired coagulation factor deficiency |
26 |
|
INPAT |
INPAT_ICD10(D818) |
Other combined immunodeficiencies |
26 |
|
OUTPAT |
OUTPAT_ICD10(D578) |
Other sickle-cell disorders |
26 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D66) |
Hereditary factor VIII deficiency. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
26 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D694) |
Other primary thrombocytopenia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
26 |
|
DEATH |
DEATH_ICD10(D860) |
Sarcoidosis of lung |
25 |
|
INPAT |
INPAT_ICD10(D598) |
Other acquired haemolytic anaemias |
25 |
|
INPAT |
INPAT_ICD10(D734) |
Cyst of spleen |
25 |
|
INPAT |
INPAT_ICD10(D738) |
Other diseases of spleen |
25 |
|
INPAT |
INPAT_ICD9(2839X) |
Acquired hemolytic anemia, unspecified |
25 |
|
INPAT |
INPAT_ICD9(2858X) |
Other specified anemias |
25 |
|
INPAT |
INPAT_ICD9(2860A) |
Congenital factor VIII disorder |
25 |
|
OUTPAT |
OUTPAT_ICD10(D595) |
Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli] |
25 |
|
OUTPAT |
OUTPAT_ICD10(D618) |
Other specified aplastic anaemias |
25 |
|
OUTPAT |
OUTPAT_ICD10(D71) |
Functional disorders of polymorphonuclear neutrophils |
25 |
|
OUTPAT |
OUTPAT_ICD10(D890) |
Polyclonal hypergammaglobulinaemia |
25 |
|
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! |
25 |
|
INPAT |
INPAT_ICD10(D8982) |
Disease caused by deposition of the light chain of the immunoglobulins |
24 |
|
INPAT |
INPAT_ICD10(D899) |
Disorder involving the immune mechanism, unspecified |
24 |
|
OUTPAT |
OUTPAT_ICD10(D513) |
Other dietary vitamin B12deficiency anaemia |
24 |
|
OUTPAT |
OUTPAT_ICD10(D561) |
Beta thalassaemia |
24 |
|
OUTPAT |
OUTPAT_ICD10(D5699) |
Thalassaemia, unspecified |
24 |
|
OUTPAT |
OUTPAT_ICD10(D600) |
Chronic acquired pure red cell aplasia |
24 |
|
OUTPAT |
OUTPAT_ICD10(D7601) |
Histiocytosis X (chronic) |
24 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D630) |
Anaemia in neoplastic disease (C00-D48+). Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
24 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D731) |
Hypersplenism. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
24 |
|
DEATH |
DEATH_ICD10(D62) |
Acute posthaemorrhagic anaemia |
23 |
|
INPAT |
INPAT_ICD10(D8418) |
Other specified defect in the complement system |
23 |
|
OUTPAT |
OUTPAT_ICD10(D5691) |
Thalassemia minor |
23 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D849) |
Immunodeficiency, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
23 |
|
INPAT |
INPAT_ICD10(D594) |
Other nonautoimmune haemolytic anaemias |
22 |
|
INPAT |
INPAT_ICD10(D70) |
Agranulocytosis |
22 |
|
INPAT |
INPAT_ICD8(28600) |
Coagulation defects, Haemophilia |
22 |
|
INPAT |
INPAT_ICD9(2830A) |
Acquired haemolytic anaemias, Autoimmune haemolytic anaemias |
22 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D580) |
Hereditary spherocytosis. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
22 |
|
DEATH |
DEATH_ICD10(D696) |
Thrombocytopenia, unspecified |
21 |
|
INPAT |
INPAT_ICD10(D730) |
Hyposplenism |
21 |
|
INPAT |
INPAT_ICD9(2811A) |
Other vitamin B12 deficiency anemia |
21 |
|
OUTPAT |
OUTPAT_ICD10(D720) |
Genetic anomalies of leukocytes |
21 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D538) |
Other specified nutritional anaemias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
21 |
|
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! |
21 |
|
DEATH |
DEATH_ICD10(D693) |
Idiopathic thrombocytopenic purpura |
20 |
|
INPAT |
INPAT_ICD8(28099) |
Name not found |
20 |
|
INPAT |
INPAT_ICD10(D750) |
Familial erythrocytosis |
19 |
|
INPAT |
INPAT_ICD10(D840) |
Lymphocyte function antigen-1 [LFA-1] defect |
19 |
|
INPAT |
INPAT_ICD8(28711) |
Purpura and other haemorrhagic conditions, Thrombocytopenia symptomatica |
19 |
|
INPAT |
INPAT_ICD9(2810A) |
Other deficiency anaemias, Pernicious anaemia |
19 |
|
OUTPAT |
OUTPAT_ICD10(D840) |
Lymphocyte function antigen-1 [LFA-1] defect |
19 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D512) |
Transcobalamin II deficiency. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
19 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D528) |
Other folate deficiency anaemias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
19 |
|
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! |
19 |
|
DEATH |
DEATH_ICD10(D591) |
Other autoimmune haemolytic anaemias |
18 |
|
INPAT |
INPAT_ICD10(D733) |
Abscess of spleen |
18 |
|
INPAT |
INPAT_ICD10(D806) |
Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia |
18 |
|
INPAT |
INPAT_ICD10(D891) |
Cryoglobulinaemia |
18 |
|
INPAT |
INPAT_ICD8(28698) |
Coagulation defects, Other |
18 |
|
INPAT |
INPAT_ICD9(2819X) |
Unspecified deficiency anemia |
18 |
|
INPAT |
INPAT_ICD9(2820A) |
Hereditary spherocytosis |
18 |
|
INPAT |
INPAT_ICD9(2872B) |
Other nonthrombocytopenic purpuras |
18 |
|
OUTPAT |
OUTPAT_ICD10(D804) |
Selective deficiency of immunoglobulin M [IgM] |
18 |
|
OUTPAT |
OUTPAT_ICD10(D824) |
Hyperimmunoglobulin E [IgE] syndrome |
18 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D619) |
Aplastic anaemia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
18 |
|
INPAT |
INPAT_ICD10(D838) |
Other common variable immunodeficiencies |
17 |
|
INPAT |
INPAT_ICD9(2883X) |
Diseases of white blood cells, Eosinophilia |
17 |
|
INPAT |
INPAT_ICD9(2888A) |
Diseases of white blood cells, Other specified disease of white blood cells |
17 |
|
OUTPAT |
OUTPAT_ICD10(D528) |
Other folate deficiency anaemias |
17 |
|
OUTPAT |
OUTPAT_ICD10(D644) |
Congenital dyserythropoietic anaemia |
17 |
|
OUTPAT |
OUTPAT_ICD10(D67) |
Hereditary factor IX deficiency |
17 |
|
OUTPAT |
OUTPAT_ICD10(D811) |
Severe combined immunodeficiency [SCID] with low T- and B-cell numbers |
17 |
|
OUTPAT |
OUTPAT_ICD10(D821) |
Di George's syndrome |
17 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D839) |
Common variable immunodeficiency, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
17 |
|
INPAT |
INPAT_ICD10(D618) |
Other specified aplastic anaemias |
16 |
|
INPAT |
INPAT_ICD10(D758) |
Other specified diseases of blood and blood-forming organs |
16 |
|
INPAT |
INPAT_ICD10(D819) |
Combined immunodeficiency, unspecified |
16 |
|
OUTPAT |
OUTPAT_ICD10(D559) |
Anaemia due to enzyme disorder, unspecified |
16 |
|
OUTPAT |
OUTPAT_ICD10(D601) |
Transient acquired pure red cell aplasia |
16 |
|
OUTPAT |
OUTPAT_ICD10(D642) |
Secondary sideroblastic anaemia due to drugs and toxins |
16 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D561) |
Beta thalassaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
16 |
|
INPAT |
INPAT_ICD10(D578) |
Other sickle-cell disorders |
15 |
|
INPAT |
INPAT_ICD10(D582) |
Other haemoglobinopathies |
15 |
|
INPAT |
INPAT_ICD10(D67) |
Hereditary factor IX deficiency |
15 |
|
INPAT |
INPAT_ICD10(D763) |
Other histiocytosis syndromes |
15 |
|
INPAT |
INPAT_ICD10(D831) |
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders |
15 |
|
OUTPAT |
OUTPAT_ICD10(D511) |
Vitamin B12deficiency anaemia due to selective vitamin B12malabsorption with proteinuria |
15 |
|
OUTPAT |
OUTPAT_ICD10(D733) |
Abscess of spleen |
15 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D800) |
Hereditary hypogammaglobulinaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
15 |
|
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! |
15 |
|
DEATH |
DEATH_ICD10(D70) |
Agranulocytosis |
14 |
|
DEATH |
DEATH_ICD10(D761) |
Haemophagocytic lymphohistiocytosis |
14 |
|
INPAT |
INPAT_ICD10(D560) |
Alpha thalassaemia |
14 |
|
INPAT |
INPAT_ICD10(D590) |
Drug-induced autoimmune haemolytic anaemia |
14 |
|
INPAT |
INPAT_ICD10(D600) |
Chronic acquired pure red cell aplasia |
14 |
|
INPAT |
INPAT_ICD10(D8413) |
Hereditary angioedema type III |
14 |
|
INPAT |
INPAT_ICD10(D890) |
Polyclonal hypergammaglobulinaemia |
14 |
|
INPAT |
INPAT_ICD9(2873X) |
Purpura and other haemorrhagic conditions, Primary thrombocytopenia |
14 |
|
INPAT |
INPAT_ICD9(2879X) |
Unspecified hemorrhagic conditions |
14 |
|
OUTPAT |
OUTPAT_ICD10(D8412) |
Hereditary angioedema type II |
14 |
|
INPAT |
INPAT_ICD10(D7601) |
Histiocytosis X (chronic) |
13 |
|
INPAT |
INPAT_ICD10(D841) |
Defects in the complement system |
13 |
|
INPAT |
INPAT_ICD8(28798) |
Purpura and other haemorrhagic conditions, Purpura et status haemorrhagicus alius |
13 |
|
OUTPAT |
OUTPAT_ICD10(D512) |
Transcobalamin II deficiency |
13 |
|
OUTPAT |
OUTPAT_ICD10(D571) |
Sickle-cell anaemia without crisis |
13 |
|
OUTPAT |
OUTPAT_ICD10(D589) |
Hereditary haemolytic anaemia, unspecified |
13 |
|
OUTPAT |
OUTPAT_ICD10(D608) |
Other acquired pure red cell aplasias |
13 |
|
OUTPAT |
OUTPAT_ICD10(D708) |
Name not found |
13 |
|
OUTPAT |
OUTPAT_ICD10(D822) |
Immunodeficiency with short-limbed stature |
13 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D609) |
Acquired pure red cell aplasia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
13 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D82) |
Immunodeficiency associated with other major defects. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
13 |
|
INPAT |
INPAT_ICD10(D51) |
Vitamin B12deficiency anaemia |
12 |
|
INPAT |
INPAT_ICD10(D561) |
Beta thalassaemia |
12 |
|
INPAT |
INPAT_ICD10(D595) |
Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli] |
12 |
|
INPAT |
INPAT_ICD10(D848) |
Other specified immunodeficiencies |
12 |
|
INPAT |
INPAT_ICD8(28390) |
Acquired haemolytic anaemias, Autoimmunisatoria primaria |
12 |
|
INPAT |
INPAT_ICD8(28500) |
Other and unspecified anaemias, Hypochromic anaemia with iron loading |
12 |
|
INPAT |
INPAT_ICD9(2890X) |
Other diseases of blood and blood-forming organs, Polycythaemia, secondary |
12 |
|
INPAT |
INPAT_ICD9(2898X) |
Other specified diseases of blood and blood-forming organs |
12 |
|
DEATH |
DEATH_ICD10(D619) |
Aplastic anaemia, unspecified |
11 |
|
INPAT |
INPAT_ICD10(D7600) |
Eosinophilic granuloma |
11 |
|
INPAT |
INPAT_ICD10(D812) |
Severe combined immunodeficiency [SCID] with low or normal B-cell numbers |
11 |
|
INPAT |
INPAT_ICD10(D8411) |
Hereditary angioedema type I |
11 |
|
INPAT |
INPAT_ICD8(28398) |
Acquired haemolytic anaemias, Aliae definitar |
11 |
|
OUTPAT |
OUTPAT_ICD10(D588) |
Other specified hereditary haemolytic anaemias |
11 |
|
OUTPAT |
OUTPAT_ICD10(D596) |
Haemoglobinuria due to haemolysis from other external causes |
11 |
|
OUTPAT |
OUTPAT_ICD10(D612) |
Aplastic anaemia due to other external agents |
11 |
|
OUTPAT |
OUTPAT_ICD10(D681) |
Hereditary factor XI deficiency |
11 |
|
OUTPAT |
OUTPAT_ICD10(D732) |
Chronic congestive splenomegaly |
11 |
|
OUTPAT |
OUTPAT_ICD10(D812) |
Severe combined immunodeficiency [SCID] with low or normal B-cell numbers |
11 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D56) |
Thalassaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
11 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D5691) |
Thalassemia minor. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
11 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D70) |
Agranulocytosis. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
11 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D735) |
Infarction of spleen. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
11 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D899) |
Disorder involving the immune mechanism, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
11 |
|
DEATH |
DEATH_ICD10(D510) |
Vitamin B12deficiency anaemia due to intrinsic factor deficiency |
10 |
|
DEATH |
DEATH_ICD10(D65) |
Disseminated intravascular coagulation [defibrination syndrome] |
10 |
|
DEATH |
DEATH_ICD10(D801) |
Nonfamilial hypogammaglobulinaemia |
10 |
|
INPAT |
INPAT_ICD10(D513) |
Other dietary vitamin B12deficiency anaemia |
10 |
|
INPAT |
INPAT_ICD10(D592) |
Drug-induced nonautoimmune haemolytic anaemia |
10 |
|
INPAT |
INPAT_ICD10(D642) |
Secondary sideroblastic anaemia due to drugs and toxins |
10 |
|
INPAT |
INPAT_ICD10(D821) |
Di George's syndrome |
10 |
|
INPAT |
INPAT_ICD10(D824) |
Hyperimmunoglobulin E [IgE] syndrome |
10 |
|
INPAT |
INPAT_ICD9(2869X) |
Other and unspecified coagulation defects |
10 |
|
OUTPAT |
OUTPAT_ICD10(D562) |
Delta-beta thalassaemia |
10 |
|
OUTPAT |
OUTPAT_ICD10(D581) |
Hereditary elliptocytosis |
10 |
|
OUTPAT |
OUTPAT_ICD10(D805) |
Immunodeficiency with increased immunoglobulin M [IgM] |
10 |
|
OUTPAT |
OUTPAT_ICD10(D828) |
Immunodeficiency associated with other specified major defects |
10 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D63) |
Anaemia in chronic diseases classified elsewhere. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
10 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D730) |
Hyposplenism. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
10 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D8411) |
Hereditary angioedema type I. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
10 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D848) |
Other specified immunodeficiencies. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
10 |
|
INPAT |
INPAT_ICD10(D528) |
Other folate deficiency anaemias |
9 |
|
INPAT |
INPAT_ICD10(D601) |
Transient acquired pure red cell aplasia |
9 |
|
INPAT |
INPAT_ICD10(D612) |
Aplastic anaemia due to other external agents |
9 |
|
INPAT |
INPAT_ICD10(D64) |
Other anaemias |
9 |
|
INPAT |
INPAT_ICD10(D813) |
Adenosine deaminase [ADA] deficiency |
9 |
|
INPAT |
INPAT_ICD10(D8419) |
Unspecified defect in the complement system |
9 |
|
INPAT |
INPAT_ICD8(28299) |
Hereditary haemolytic anaemias, Other |
9 |
|
INPAT |
INPAT_ICD8(28404) |
Aplastic anaemia, Erythroblastopenia acquisita |
9 |
|
INPAT |
INPAT_ICD9(2874X) |
Purpura and other haemorrhagic conditions, Secondary thrombocytopenia |
9 |
|
INPAT |
INPAT_ICD9(2880X) |
Diseases of white blood cells, Agranulocytosis |
9 |
|
INPAT |
INPAT_ICD9(2899X) |
Unspecified diseases of blood and blood-forming organs |
9 |
|
OUTPAT |
OUTPAT_ICD10(D592) |
Drug-induced nonautoimmune haemolytic anaemia |
9 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D560) |
Alpha thalassaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
9 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D5699) |
Thalassaemia, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
9 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D610) |
Constitutional aplastic anaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
9 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D830) |
Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
9 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D8413) |
Hereditary angioedema type III. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
9 |
|
DEATH |
DEATH_ICD10(D862) |
Sarcoidosis of lung with sarcoidosis of lymph nodes |
8 |
|
INPAT |
INPAT_ICD10(D589) |
Hereditary haemolytic anaemia, unspecified |
8 |
|
INPAT |
INPAT_ICD10(D596) |
Haemoglobinuria due to haemolysis from other external causes |
8 |
|
INPAT |
INPAT_ICD10(D644) |
Congenital dyserythropoietic anaemia |
8 |
|
INPAT |
INPAT_ICD10(D828) |
Immunodeficiency associated with other specified major defects |
8 |
|
INPAT |
INPAT_ICD10(D892) |
Hypergammaglobulinaemia, unspecified |
8 |
|
INPAT |
INPAT_ICD8(28120) |
Other vitamin B12 deficiency anaemia, Folic acid deficiency anaemia |
8 |
|
INPAT |
INPAT_ICD8(28198) |
Other anaemia, Alia definita |
8 |
|
INPAT |
INPAT_ICD8(28409) |
Aplastic anaemia, Unspecified |
8 |
|
INPAT |
INPAT_ICD8(28610) |
Coagulation defects, Christmas disease |
8 |
|
INPAT |
INPAT_ICD9(2830X) |
Acquired haemolytic anaemias, Autoimmune haemolytic anaemias |
8 |
|
OUTPAT |
OUTPAT_ICD10(D570) |
Sickle-cell anaemia with crisis |
8 |
|
OUTPAT |
OUTPAT_ICD10(D749) |
Methaemoglobinaemia, unspecified |
8 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D501) |
Sideropenic dysphagia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
8 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D593) |
Haemolytic-uraemic syndrome. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
8 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D594) |
Other nonautoimmune haemolytic anaemias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
8 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D7081) |
Neutropenia congenital. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
8 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D739) |
Disease of spleen, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
8 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D841) |
Defects in the complement system. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
8 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D891) |
Cryoglobulinaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
8 |
|
DEATH |
DEATH_ICD10(D599) |
Acquired haemolytic anaemia, unspecified |
7 |
|
INPAT |
INPAT_ICD10(D521) |
Drug-induced folate deficiency anaemia |
7 |
|
INPAT |
INPAT_ICD10(D570) |
Sickle-cell anaemia with crisis |
7 |
|
INPAT |
INPAT_ICD10(D71) |
Functional disorders of polymorphonuclear neutrophils |
7 |
|
INPAT |
INPAT_ICD10(D720) |
Genetic anomalies of leukocytes |
7 |
|
INPAT |
INPAT_ICD10(D822) |
Immunodeficiency with short-limbed stature |
7 |
|
INPAT |
INPAT_ICD10(D86) |
Sarcoidosis |
7 |
|
INPAT |
INPAT_ICD8(28402) |
Aplastic anaemia, Acquisita secundaria |
7 |
|
INPAT |
INPAT_ICD8(28588) |
Other and unspecified anaemias, Other specified anaemia |
7 |
|
INPAT |
INPAT_ICD9(2870X) |
Purpura and other haemorrhagic conditions, Allergic purpura |
7 |
|
INPAT |
INPAT_ICD9(2878X) |
Other specified hemorrhagic conditions |
7 |
|
INPAT |
INPAT_ICD9(2880A) |
Diseases of white blood cells, Agranulocytosis |
7 |
|
INPAT |
INPAT_ICD9(2888X) |
Diseases of white blood cells, Other specified disease of white blood cells |
7 |
|
OUTPAT |
OUTPAT_ICD10(D550) |
Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency |
7 |
|
OUTPAT |
OUTPAT_ICD10(D568) |
Other thalassaemias |
7 |
|
OUTPAT |
OUTPAT_ICD10(D75) |
Other diseases of blood and blood-forming organs |
7 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D641) |
Secondary sideroblastic anaemia due to disease. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
7 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D684) |
Acquired coagulation factor deficiency. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
7 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D763) |
Other histiocytosis syndromes. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
7 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D824) |
Hyperimmunoglobulin E [IgE] syndrome. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
7 |
|
DEATH |
DEATH_ICD10(D593) |
Haemolytic-uraemic syndrome |
6 |
|
DEATH |
DEATH_ICD10(D695) |
Secondary thrombocytopenia |
6 |
|
DEATH |
DEATH_ICD10(D728) |
Other specified disorders of white blood cells |
6 |
|
DEATH |
DEATH_ICD10(D752) |
Essential thrombocytosis |
6 |
|
INPAT |
INPAT_ICD10(D5699) |
Thalassaemia, unspecified |
6 |
|
INPAT |
INPAT_ICD10(D573) |
Sickle-cell trait |
6 |
|
INPAT |
INPAT_ICD10(D681) |
Hereditary factor XI deficiency |
6 |
|
INPAT |
INPAT_ICD10(D811) |
Severe combined immunodeficiency [SCID] with low T- and B-cell numbers |
6 |
|
INPAT |
INPAT_ICD10(D829) |
Immunodeficiency associated with major defect, unspecified |
6 |
|
INPAT |
INPAT_ICD8(28100) |
Other anaemia, Perniciosa cum myelopathia spinali |
6 |
|
INPAT |
INPAT_ICD8(28391) |
Acquired haemolytic anaemias, Autoimmunisatoria secundaria |
6 |
|
INPAT |
INPAT_ICD8(28730) |
Purpura and other haemorrhagic conditions, Thrombocytopathy |
6 |
|
INPAT |
INPAT_ICD9(2848D) |
Aplastic anaemia, Other specified aplastic anaemias |
6 |
|
INPAT |
INPAT_ICD9(2848X) |
Aplastic anaemia, Other specified aplastic anaemias |
6 |
|
INPAT |
INPAT_ICD9(2867X) |
Coagulation defects, Acquired coagulation factor deficiency |
6 |
|
INPAT |
INPAT_ICD9(2873C) |
Purpura and other haemorrhagic conditions, Primary thrombocytopenia |
6 |
|
INPAT |
INPAT_ICD9(2889X) |
Unspecified disease of white blood cells |
6 |
|
INPAT |
INPAT_ICD9(2895A) |
Other diseases of spleen |
6 |
|
OUTPAT |
OUTPAT_ICD10(D521) |
Drug-induced folate deficiency anaemia |
6 |
|
OUTPAT |
OUTPAT_ICD10(D538) |
Other specified nutritional anaemias |
6 |
|
OUTPAT |
OUTPAT_ICD10(D760) |
Langerhans' cell histiocytosis, not elsewhere classified |
6 |
|
OUTPAT |
OUTPAT_ICD10(D820) |
Wiskott-Aldrich syndrome |
6 |
|
OUTPAT |
OUTPAT_ICD10(D832) |
Common variable immunodeficiency with autoantibodies to B- or T-cells |
6 |
|
OUTPAT |
OUTPAT_ICD10(D8414) |
C1 esterase inhibitor deficiency (C1-INH deficiency) |
6 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D571) |
Sickle-cell anaemia without crisis. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
6 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D59) |
Acquired haemolytic anaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
6 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D595) |
Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli]. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
6 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D608) |
Other acquired pure red cell aplasias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
6 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D613) |
Idiopathic aplastic anaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
6 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D67) |
Hereditary factor IX deficiency. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
6 |
|
DEATH |
DEATH_ICD10(D519) |
Vitamin B12deficiency anaemia, unspecified |
5 |
|
DEATH |
DEATH_ICD10(D648) |
Other specified anaemias |
5 |
|
DEATH |
DEATH_ICD10(D688) |
Other specified coagulation defects |
5 |
|
DEATH |
DEATH_ICD10(D735) |
Infarction of spleen |
5 |
|
INPAT |
INPAT_ICD10(D511) |
Vitamin B12deficiency anaemia due to selective vitamin B12malabsorption with proteinuria |
5 |
|
INPAT |
INPAT_ICD10(D538) |
Other specified nutritional anaemias |
5 |
|
INPAT |
INPAT_ICD10(D563) |
Thalassaemia trait |
5 |
|
INPAT |
INPAT_ICD10(D608) |
Other acquired pure red cell aplasias |
5 |
|
INPAT |
INPAT_ICD10(D732) |
Chronic congestive splenomegaly |
5 |
|
INPAT |
INPAT_ICD10(D762) |
Haemophagocytic syndrome, infection-associated |
5 |
|
INPAT |
INPAT_ICD10(D805) |
Immunodeficiency with increased immunoglobulin M [IgM] |
5 |
|
INPAT |
INPAT_ICD10(D820) |
Wiskott-Aldrich syndrome |
5 |
|
INPAT |
INPAT_ICD8(28001) |
Name not found |
5 |
|
INPAT |
INPAT_ICD8(28300) |
Acquired haemolytic anaemias, Acute |
5 |
|
INPAT |
INPAT_ICD8(28559) |
Name not found |
5 |
|
INPAT |
INPAT_ICD9(2850X) |
Other and unspecified anaemias, Sideroblastic anaemia |
5 |
|
INPAT |
INPAT_ICD9(2890A) |
Other diseases of blood and blood-forming organs, Polycythaemia, secondary |
5 |
|
OUTPAT |
OUTPAT_ICD10(D552) |
Anaemia due to disorders of glycolytic enzymes |
5 |
|
OUTPAT |
OUTPAT_ICD10(D72) |
Other disorders of white blood cells |
5 |
|
OUTPAT |
OUTPAT_ICD10(D829) |
Immunodeficiency associated with major defect, unspecified |
5 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D578) |
Other sickle-cell disorders. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
5 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D598) |
Other acquired haemolytic anaemias. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
5 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D640) |
Hereditary sideroblastic anaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
5 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D738) |
Other diseases of spleen. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
5 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D760) |
Langerhans' cell histiocytosis, not elsewhere classified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
5 |
|
PRIM_OUT |
PRIM_OUT_NOT_USED_ICD10(D838) |
Other common variable immunodeficiencies. 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(D8419) |
Unspecified defect in the complement system. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! |
5 |
|