Disorder of cellular component of blood + all descendants
Metadata
- Coding system
- SNOMED CT (UK Clinical Edition)
- Coding system release
- unknown
- Author
- Kate Mansfield
- Codelist ID
- user/kate-mansfield/disorder-of-cellular-component-of-blood-all-descendants
- Version ID
- 611a2102
- Number of codes included
- 1,065
About
Description
Disorder of cellular component of blood (`414022008`) and all descendants.
Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.
We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.
| code | term |
|---|---|
| 1003381002 | Onycho-tricho-dysplasia neutropenia syndrome |
| 1003473002 | B cell lymphocyte aplasia caused by drug |
| 1010397000 | Severe deficiency of glucose-6-phosphate dehydrogenase |
| 10205009 | Megaloblastic anemia due to exfoliative dermatitis |
| 10294000 | Reactive mastocytosis |
| 105599000 | Anemia related to disturbed deoxyribonucleic acid synthesis |
| 105600002 | Disorder of neutrophils |
| 105601003 | Quantitative disorder of neutrophils |
| 105602005 | Quantitative abnormality of granulocytes |
| 105603000 | Non-malignant lymphocyte AND/OR plasma cell disorder |
| 10564005 | Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin |
| 10619002 | Megaloblastic anemia due to poor nutrition |
| 10741751000119100 | Anemia in mother complicating childbirth |
| 10752381000119101 | Fetal thrombocytopenia |
| 10759351000119103 | Sickle cell anemia in mother complicating childbirth |
| 10759401000119105 | Sickle cell trait in mother complicating childbirth |
| 10762261000119105 | Anemia following acute postoperative blood loss |
| 10806241000119108 | Thalassemia in mother complicating childbirth |
| 10812081000119108 | Iron deficiency anemia in mother complicating childbirth |
| 109994006 | Essential thrombocythemia |
| 109996008 | Myelodysplastic syndrome: Refractory anemia, without ringed sideroblasts, without excess blasts |
| 109998009 | Refractory anemia with ringed sideroblasts |
| 110000005 | Refractory anemia with excess blasts in transformation |
| 111037009 | Basophilic hyperplasia |
| 111396008 | Chédiak-Higashi syndrome |
| 111407006 | Hemolytic uremic syndrome |
| 111469006 | Hemolytic disease of the newborn due to non-ABO, non-Rh isoimmunization |
| 111570005 | Anemia due to infection |
| 111571009 | Congenital atransferrinemia |
| 111572002 | beta^0^ Thalassemia, nondeletion type |
| 111574001 | Anemia due to copper deficiency |
| 111575000 | Anemia due to membrane defect |
| 111576004 | Acquired stomatocytosis |
| 111577008 | Anemia due to enzyme deficiency |
| 111578003 | Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency |
| 111579006 | Hereditary nonspherocytic hemolytic anemia due to glutathione synthetase deficiency |
| 111581008 | Anemia caused by physical agent |
| 111583006 | Leukocytosis |
| 111584000 | Reticular dysgenesis |
| 111585004 | Neutropenia associated with autoimmune disease |
| 111588002 | Heparin-induced thrombocytopenia with thrombosis |
| 11376001 | Hereditary acanthocytosis |
| 11491000 | Anemia due to niacin deficiency |
| 11503009 | Relative anemia |
| 115963009 | Regenerative anemia |
| 11781007 | Autoimmune hemolytic anemia caused by complement |
| 118791000119106 | Aplastic anemia caused by antineoplastic agent |
| 12189000 | Coombs negative hemolytic anemia |
| 12238007 | Megaloblastic anemia due to gastrectomy |
| 123767004 | Hemoglobinemia |
| 123772008 | Homozygous hemoglobinopathy |
| 123773003 | Heterozygous hemoglobinopathy |
| 123777002 | Autoimmune leukopenia |
| 1239371000000103 | Haemoglobin E beta zero thalassaemia |
| 1239381000000101 | Haemoglobin E beta plus thalassaemia |
| 124134002 | Deficiency of glucose-6-phosphate dehydrogenase |
| 124188007 | Deficiency of glutathione reductase (reduced nicotinamide adenine dinucleotide phosphate) |
| 124297004 | Deficiency of hexokinase |
| 127034005 | Pancytopenia |
| 127037003 | Toxic methemoglobinemia with cyanosis |
| 127038008 | Hereditary hemoglobinopathy due to globin chain mutation |
| 127039000 | Acquired hemoglobinopathy |
| 127040003 | Sickle cell-hemoglobin SS disease |
| 127041004 | Sickle cell-beta-thalassemia |
| 127042006 | Sickle cell beta plus thalassemia |
| 127043001 | Sickle cell-beta^0^-thalassemia |
| 127044007 | Sickle cell-delta beta^0^-thalassemia |
| 127045008 | Sickle cell anemia with coexistent alpha-thalassemia |
| 127046009 | Sickle cell trait with coexistent alpha-thalassemia |
| 127047000 | Sickle cell-hemoglobin Lepore disease |
| 127048005 | Sickle cell-Hemoglobin O Arab disease |
| 127049002 | Primary (idiopathic) autoimmune hemolytic anemia |
| 127050002 | Secondary autoimmune hemolytic anemia |
| 127052005 | Secondary warm autoimmune hemolytic anemia |
| 127053000 | Post-infectious cold agglutinin disease |
| 127054006 | Cold agglutinin disease caused by Epstein-Barr virus infection |
| 127055007 | Chronic cold agglutinin disease |
| 127056008 | Chronic cold agglutinin disease associated with B-cell neoplasm |
| 127057004 | Paroxysmal cold hemoglobinuria |
| 127058009 | Paroxysmal cold hemoglobinuria associated with tertiary syphilis |
| 127060006 | Drug-induced immune hemolytic anemia, hapten type |
| 127061005 | Autoimmune hemolytic anemia, categorized by antibody class AND/OR complement |
| 127062003 | Erythrocytosis |
| 127063008 | Erythrocytosis due to cyanotic congenital heart disease |
| 127065001 | Familial erythrocytosis due to diphosphoglycerate mutase deficiency |
| 127066000 | Familial polycythemia vera |
| 127067009 | Stress neutrophilia |
| 127218004 | Reactive follicular hyperplasia in the elderly |
| 127319005 | Anemia caused by alloimmune destruction of transfused red cells |
| 128086004 | Hemolytic disorder |
| 128090002 | Benign gestational thrombocytopenia |
| 128091003 | Autoimmune thrombocytopenia |
| 128092005 | Secondary autoimmune thrombocytopenia |
| 128093000 | Alloimmune thrombocytopenia |
| 128094006 | Alloimmune platelet transfusion refractoriness |
| 128095007 | Acquired platelet function disorder |
| 128096008 | Hereditary platelet function disorder |
| 128098009 | Scott syndrome |
| 128099001 | Platelet storage pool defect |
| 128100009 | Mixed alpha granule and dense body deficiency |
| 128101008 | Platelet factor V deficiency (factor V Quebec) |
| 128102001 | Familial alpha>2< adrenergic receptor defect in platelets |
| 128103006 | Isolated collagen aggregation defect |
| 12814002 | B lymphocyte disorder |
| 12907000 | Thiamine-responsive megaloblastic anemia |
| 129638002 | Hemolytic anemia caused by hyperbaric oxygen |
| 129639005 | Hereditary neutrophilia |
| 129640007 | Benign granulocytopenia in childhood |
| 129641006 | Chronic benign neutropenia of childhood |
| 129642004 | Chronic idiopathic immunoneutropenia in adults |
| 129643009 | Chronic hypoplastic neutropenia |
| 129644003 | Myeloperoxidase deficiency syndrome |
| 129645002 | Adult glucose-6-phosphate dehydrogenase deficiency of leukocytes syndrome |
| 129654004 | Acquired platelet factor 3 disease |
| 13172003 | Chronic idiopathic thrombocytopenic purpura |
| 14024008 | Humoral immunologic aplastic anemia |
| 14087004 | Hereditary stomatocytosis |
| 14126008 | Autosomal-linked pyridoxine refractory sideroblastic anemia |
| 14333004 | Alloimmune neonatal neutropenia |
| 14379009 | Dimorphic anemia |
| 14514008 | Anemia due to disturbance of hemoglobin synthesis |
| 15012007 | Granulocyte abnormality due to immune defect |
| 15121005 | Hereditary elliptocytosis due to glycophorin C deficiency |
| 15276008 | Drug-induced enzyme deficiency anemia |
| 15326009 | beta^+^ Thalassemia, normal Hb A>2<, type 2 |
| 15332004 | Goats' milk anemia |
| 15466007 | Erythrocytosis due to cerebellar hemangioma |
| 154826009 | Secondary thrombocytopenia |
| 16360009 | Delta beta thalassemia |
| 16402000 | Sickle cell trait |
| 16427007 | Delta thalassemia |
| 165531008 | Lymphocytosis - absolute |
| 16623961000119100 | Pancytopenia caused by immunosuppressant |
| 16645003 | Anemia caused by insect venom |
| 16697871000119100 | Mast cell activation syndrome |
| 16964007 | Hereditary persistence of fetal hemoglobin thalassemia |
| 17182001 | Agranulocytosis |
| 17342003 | Familial erythrocytosis |
| 17592003 | Platelet dysfunction caused by aspirin |
| 1801000119106 | Anemia, pre-end stage renal disease on erythropoietin protocol |
| 18273004 | Unstable hemoglobin disease |
| 183005 | Autoimmune pancytopenia |
| 18323000 | Drug-induced immune hemolytic anemia, immune complex type |
| 18637002 | Megaloblastic anemia of premature infant |
| 18662002 | Acquired Heinz body anemia |
| 189509003 | Refractory anemia without sideroblasts, so stated |
| 190959006 | Hemophagocytic lymphohistiocytosis due to infection |
| 190996002 | Severe combined immunodeficiency with reticular dysgenesis |
| 191128004 | Iron deficiency anemia due to dietary causes |
| 191136008 | Idiopathic hypochromic anemia |
| 191142007 | Vitamin B12 deficiency anemia due to malabsorption with proteinuria |
| 191146005 | Congenital folate malabsorption anemia |
| 191148006 | Folate deficiency anemia, drug-induced |
| 191149003 | Folate deficiency anemia due to malabsorption |
| 191150003 | Folate deficiency anemia due to liver disorders |
| 191154007 | Combined B12 and folate deficiency anemia |
| 191161006 | Vitamin C deficiency anemia |
| 191169008 | Hereditary elliptocytosis |
| 191170009 | Hemolytic anemia due to glutathione metabolism disorder |
| 191172001 | Favism |
| 191177007 | Hemolytic anemia due to hexokinase deficiency |
| 191178002 | Hemolytic anemia due to pyruvate kinase deficiency |
| 191179005 | Hemolytic anemia due to triose phosphate isomerase deficiency |
| 191180008 | Anemia due to disorders of nucleotide metabolism |
| 191187006 | Alpha trait thalassemia |
| 191189009 | Beta thalassemia intermedia |
| 191201002 | Hereditary persistence of fetal hemoglobin |
| 191202009 | Hemoglobin Zurich disease |
| 191210005 | Primary cold-type hemolytic anemia |
| 191211009 | Primary warm-type hemolytic anemia |
| 191212002 | Secondary cold-type hemolytic anemia |
| 191213007 | Secondary warm-type hemolytic anemia |
| 191216004 | Non-autoimmune hemolytic anemia |
| 191217008 | Mechanical hemolytic anemia |
| 191218003 | Toxic hemolytic anemia |
| 191222008 | Hemoglobinuria due to hemolysis from external causes |
| 191228007 | Acquired spherocytosis |
| 191229004 | Pyknocytosis, infantile |
| 191244003 | Aplastic anemia due to chronic disease |
| 191246001 | Aplastic anemia due to infection |
| 191247005 | Aplastic anemia caused by radiation |
| 191248000 | Aplastic anemia caused by toxic cause |
| 191251007 | Transient hypoplastic anemia |
| 191255003 | Transient acquired pure red cell aplasia |
| 191256002 | Idiopathic aplastic anemia |
| 191260004 | Pyridoxine-responsive sideroblastic anemia |
| 191261000 | Secondary sideroblastic anemia due to disease |
| 191262007 | Secondary sideroblastic anemia caused by drugs and toxins |
| 191265009 | Anemia in neoplastic disease |
| 191268006 | Chronic anemia |
| 191273000 | Leukemoid reaction of the newborn |
| 191322006 | Thrombocytopenia caused by drugs |
| 191323001 | Thrombocytopenia due to extracorporeal circulation of blood |
| 191338000 | Primary splenic neutropenia |
| 191345000 | Acquired neutropenia in newborn |
| 191347008 | Cyclical neutropenia |
| 191358004 | Hereditary eosinophilia |
| 191360002 | Drug-induced eosinophilia |
| 191372008 | Polycythemia due to cyanotic heart disease |
| 191373003 | Polycythemia due to cyanotic respiratory disease |
| 191388008 | Familial methemoglobinemia |
| 191389000 | Idiopathic methemoglobinemia |
| 191390009 | Drug-induced methemoglobinemia |
| 19307009 | Drug-induced immune thrombocytopenia |
| 19442009 | Heterozygous thalassemia |
| 19588001 | Erythrocytosis due to tissue hypoxemia |
| 1963002 | Paroxysmal nocturnal hemoglobinuria |
| 19636003 | Monocytosis |
| 198830009 | Intravascular hemolysis following abortive pregnancy |
| 199244000 | Anemia during pregnancy - baby delivered |
| 199245004 | Anemia in the puerperium - baby delivered during current episode of care |
| 199246003 | Anemia during pregnancy - baby not yet delivered |
| 199247007 | Anemia in the puerperium - baby delivered during previous episode of care |
| 199248002 | Iron deficiency anemia of pregnancy |
| 206434001 | Late anemia of newborn due to isoimmunization |
| 206510008 | Transient neonatal thrombocytopenia due to exchange transfusion |
| 206511007 | Transient neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia |
| 206512000 | Transient neonatal thrombocytopenia due to isoimmunization |
| 21043008 | Neutrophil cytomatrix disorder |
| 21412009 | X chromosome-linked pyridoxine refractory sideroblastic anemia |
| 21527007 | Chronic granulomatous disease, type IV |
| 21914002 | Anemia of thyroid dysfunction |
| 22098000 | Chronic idiopathic autoimmune hemolytic anemia |
| 22310002 | Chronic idiopathic monocytosis |
| 22347002 | Anemia of gonadal dysfunction |
| 22438006 | Anemia due to disturbance of proliferation AND/OR differentiation of hematopoietic stem cells |
| 22716005 | Platelet disorder |
| 22933009 | Glucose-6-phosphate dehydrogenase deficiency class I variant anemia |
| 23205009 | Transient neonatal thrombocytopenia |
| 23269001 | Double heterozygous sickling disorder |
| 233691007 | Asthmatic pulmonary eosinophilia |
| 233692000 | Cryptogenic pulmonary eosinophilia |
| 23371004 | Epsilon gamma delta beta thalassemia |
| 234338001 | Non-anemic red cell disorder |
| 234339009 | Macrocytosis - no anemia |
| 234340006 | Iron deficiency without anemia |
| 234341005 | Alcohol-related macrocytosis |
| 234343008 | Normocytic anemia due to aplasia |
| 234345001 | von Jaksch's anemia |
| 234346000 | Dilutional anemia |
| 234347009 | Anemia of chronic disorder |
| 234348004 | Anemia of renal disease |
| 234349007 | Microcytic anemia |
| 234350007 | Neonatal anemia |
| 234352004 | Normocytic anemia due to chronic blood loss |
| 234353009 | Congenital transferrin deficiency |
| 234358000 | Megaloblastic anemia due to dietary causes |
| 234360003 | Vegan's anemia |
| 234361004 | Congenital deficiency of intrinsic factor |
| 234362006 | Biermer's congenital pernicious anemia |
| 234363001 | Selective malabsorption of cyanocobalamin |
| 234364007 | Combined deficiency anemia |
| 234365008 | Thiamine-responsive macrocytosis |
| 234366009 | Alcohol-related sideroblastic anemia |
| 234367000 | Pancytopenia with pancreatitis |
| 234370001 | Pure red cell aplasia, acquired |
| 234375006 | Transient erythroblastopenia of childhood |
| 234376007 | Acquired red cell aplasia |
| 234380002 | Kell isoimmunization of the newborn |
| 234381003 | Maternal autoimmune hemolytic anemia |
| 234383000 | Homozygous alpha thalassemia |
| 234385007 | Alpha thalassemia-2 trait |
| 234386008 | Hemoglobin Constant Spring trait |
| 234387004 | Hemoglobin Lepore trait |
| 234388009 | Delta-beta-Lepore thalassemia |
| 234389001 | Alpha-beta thalassemia |
| 234390005 | Gamma thalassemia |
| 234391009 | Sickle cell anemia with high hemoglobin F |
| 234392002 | Hemoglobin E/beta thalassemia disease |
| 234393007 | Low affinity hemoglobin |
| 234394001 | High affinity hemoglobin |
| 234395000 | Congenital methemoglobinaema with defective methemoglobin-reducing system |
| 234396004 | Congenital methemoglobinemia with abnormal methemoglobins |
| 234400004 | Secondary polycythemia without excess erythropoietin |
| 234401000 | Erythrocyte enzyme deficiency |
| 234402007 | Chronic non-spherocytic hemolytic anemia |
| 234403002 | Phosphoglycerokinase deficiency |
| 234404008 | Glucose phosphate isomerase deficiency |
| 234405009 | Triose phosphate isomerase deficiency |
| 234407001 | Uridine monophosphate hydrolase deficiency |
| 234408006 | Adenosine deaminase overproduction |
| 234409003 | Erythrocyte membrane abnormality |
| 234410008 | Hereditary elliptocytosis with transient poikilocytosis |
| 234411007 | Blood group deletion syndrome |
| 234412000 | Abnormal cation transport syndrome |
| 234413005 | Alpha/beta lipoproteinemia |
| 234414004 | Non-malignant white cell disorder |
| 234416002 | X-linked hypogammaglobulinemia |
| 234417006 | T-cell lymphocytosis |
| 234418001 | Chronic benign granulocytopenia |
| 234423001 | Chronic benign neutropenia |
| 234424007 | Metabolic neutropenia |
| 234425008 | Autoimmune neutropenia |
| 234426009 | Corticosteroid-induced neutrophilia |
| 234427000 | Monocytoid disorder |
| 234428005 | Lymphocytoid disorder |
| 234429002 | Chemotactic disorder |
| 234430007 | CR3-receptor deficiency |
| 234431006 | Specific granule deficiency |
| 234433009 | Myeloperoxidase deficiency |
| 234434003 | Alders syndrome |
| 234435002 | Hereditary hypersegmentation |
| 234436001 | Hemolytic erythrophagocytic syndrome |
| 234437005 | Hemophagocytic lymphohistiocytosis |
| 234469001 | Inherited platelet disorder |
| 234470000 | Platelet membrane defect |
| 234471001 | Glycoprotein Ia defect |
| 234472008 | Glycoprotein Ib defect |
| 234473003 | Platelet type von Willebrand's disease |
| 234474009 | Dense body defect |
| 234475005 | Thromboxane generation defect |
| 234476006 | Cyclooxygenase deficiency |
| 234477002 | Thromboxane synthetase deficiency |
| 234478007 | Giant platelet syndrome |
| 234479004 | Acquired platelet disorder |
| 234482009 | Amegakaryocytic thrombocytopenia |
| 234483004 | Megakaryocytic thrombocytopenia |
| 234484005 | May-Hegglin anomaly |
| 234485006 | Epstein syndrome |
| 234486007 | Montreal platelet syndrome |
| 234487003 | Mediterranean thrombocytopenia |
| 234500001 | Reactive thrombocytosis |
| 234512002 | Post-splenectomy thrombocytosis |
| 234513007 | Post-splenectomy leukocytosis |
| 234576008 | Chronic familial neutropenia |
| 234582006 | Leukocyte adhesion deficiency - type 1 |
| 234583001 | Leukocyte adhesion deficiency - type 2 |
| 234587000 | Neutrophil lactoferrin deficiency |
| 234588005 | Neutrophil secondary granule deficiency |
| 234589002 | Glutathione synthetase deficiency |
| 234590006 | Gluthathione peroxidase deficiency |
| 234591005 | Combined phagocytic defect |
| 237617006 | Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness |
| 237985009 | Pearson's syndrome |
| 238091006 | Lecithin cholesterol acyltransferase deficiency |
| 238092004 | Fish-eye disease |
| 238931006 | Eosinophilic cellulitis |
| 239910001 | Toxic oil syndrome |
| 240305000 | Neonatal thrombocytopenia due to platelet alloimmunization |
| 240453002 | Oroya fever |
| 240486003 | Parvoviral aplastic crisis |
| 24159007 | Persistent lymphocytosis |
| 241954008 | Idiopathic anaphylaxis |
| 24620004 | Hemolytic anemia caused by babesiosis |
| 24661004 | Glucose-6-phosphate dehydrogenase deficiency class III variant anemia |
| 247860002 | Familial neutropenia |
| 24829000 | Eosinophilic ulcerative colitis |
| 248693006 | Chronic idiopathic neutropenia |
| 24962009 | Anemia due to vitamin E deficiency |
| 24974008 | Myelokathexis |
| 24975009 | Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin |
| 25065001 | Hemoglobin E disease |
| 25251008 | Hereditary nonspherocytic hemolytic anemia due to gamma glutamyl cysteine synthetase deficiency |
| 25266006 | Hereditary spherocytosis due to spectrin deficiency |
| 25443007 | X chromosome-linked pyridoxine responsive sideroblastic anemia |
| 25472008 | Sickle cell-hemoglobin D disease |
| 25502009 | Episodic lymphocytopenia |
| 25601009 | Erythrocytosis due to autotransfusion |
| 25881005 | Erythrocytosis caused by low atmospheric pressure |
| 26252007 | Chronic granulomatous disease, type IIA |
| 26333003 | Megaloblastic anemia due to vitamin B>12< malabsorption with proteinuria |
| 26409005 | Congenital dyserythropoietic anemia, type III |
| 26682008 | Homozygous beta thalassemia |
| 267454002 | Acatalasemia |
| 267513007 | Deficiency anemias |
| 267517008 | Vitamin B12 deficiency anemia due to dietary causes |
| 267518003 | Folate deficiency anemia due to dietary causes |
| 267524009 | Constitutional aplastic anemia with malformation |
| 267527002 | Aplastic anemia due to drugs |
| 267530009 | Acute posthemorrhagic anemia |
| 267532001 | Qualitative platelet disorder |
| 267534000 | Primary thrombocytopenia |
| 267535004 | Congenital thrombocytopenic purpura |
| 267540007 | Neutropenia caused by irradiation |
| 267550008 | Congenital methemoglobinemia |
| 26848004 | Chorea acanthocytosis syndrome |
| 269175006 | Beta thalassemia trait |
| 2694001 | Myelophthisic anemia |
| 26944003 | Acute megaloblastic anemia due to dialysis |
| 270117002 | Platelet type pseudo-von Willebrand disease |
| 27080008 | beta^0^ Thalassemia, deletion type |
| 271737000 | Anemia |
| 27342004 | Anemia of pregnancy |
| 27366005 | Megaloblastic anemia due to hemodialysis |
| 273985002 | Anemia due to isoimmunization |
| 273986001 | Perinatal thrombocytopenia |
| 275523003 | Pancytopenia-dysmelia |
| 276268001 | T-cell mediated cytopenia |
| 276448005 | Idiopathic sideroblastic anemia |
| 276575001 | Autoimmune neonatal thrombocytopenia |
| 276576000 | Neutropenia of the small for gestational age baby |
| 276578004 | Physiological anemia of infancy |
| 276579007 | Late anemia of newborn |
| 276580005 | Atypical isoimmunization of newborn |
| 276628009 | Chloramphenicol-induced neutropenia |
| 277543005 | Malignant white blood cell disorder |
| 27798002 | Megaloblastic anemia due to impaired absorption of folate |
| 278363000 | Alcoholic macrocytosis |
| 278484009 | Tropical pulmonary eosinophilia |
| 28147001 | Hemolytic anemia caused by Clostridium welchii |
| 28319009 | Erythrocytosis due to cardiovascular disease |
| 2835000 | Traumatic cardiac hemolytic anemia |
| 28505005 | Acute idiopathic thrombocytopenic purpura |
| 285777008 | Idiopathic erythrocytosis |
| 286928002 | Deficiency anemias, excluding iron |
| 288327009 | Granulation anomaly |
| 289317009 | Granulocyte granule deficiency |
| 2897005 | Immune thrombocytopenia |
| 28975000 | Constitutional aplastic anemia |
| 290246007 | Sideropenic anemia with reticuloendothelial siderosis |
| 29120000 | Eosinophilic colitis |
| 291262006 | Simple chronic anemia |
| 29177004 | Anemia due to pentose phosphate pathway defect |
| 29272001 | Chronic granulomatous disease, type I |
| 294303000 | Acquired methemoglobinuria |
| 295315008 | Acquired methemoglobinemia |
| 29551000 | Anemia caused by oxygen |
| 296332004 | Acquired storage pool deficiency (platelets) |
| 297307009 | Exhausted platelets |
| 29789008 | Monocytic leukemoid reaction |
| 2990008 | Lymphocytic leukemoid reaction |
| 300980002 | Normocytic anemia |
| 301317008 | Hereditary nonspherocytic hemolytic anemia |
| 30182008 | Thrombocytopenia due to extracorporeal circulation |
| 302215000 | Thrombocytopenic disorder |
| 302873008 | Thrombocytopenic purpura |
| 303011007 | Neutropenic disorder |
| 303060002 | Normocytic anemia following acute bleed |
| 30418008 | Anemia of adrenal dysfunction |
| 30575002 | Fanconi's anemia |
| 306058006 | Aplastic anemia |
| 307333004 | Rhesus isoimmunization due to anti-D |
| 307334005 | Rhesus isoimmunization due to anti-c |
| 307335006 | Rhesus isoimmunization due to anti-E |
| 307336007 | Rhesus isoimmunization due to anti-Cw |
| 307337003 | Duffy isoimmunization of the newborn |
| 307338008 | Kidd isoimmunization of the newborn |
| 307342006 | Thrombocytopenia due to massive blood transfusion |
| 307343001 | Acquired hemoglobin H disease |
| 307592006 | Basophilic leukemia |
| 307726001 | Anemia in ovarian carcinoma |
| 309742004 | Drug-induced autoimmune hemolytic anemia |
| 30981000 | Secondary eosinophilia |
| 310647000 | Anemia secondary to renal failure |
| 31206006 | Refractory megaloblastic anemia |
| 313291009 | Anemia during the puerperium |
| 317226009 | Granulocytosis |
| 31820007 | Anemia of endocrine disorder |
| 319171004 | Qualitative abnormality of granulocyte |
| 320150004 | Idiopathic eosinophilia |
| 32092008 | Toxic neutropenia |
| 32094009 | Megaloblastic anemia caused by fish tapeworm |
| 32117000 | Sulfhemoglobinemia |
| 322096003 | Platelet sequestration |
| 322699009 | Intracorpuscular hemolytic anemia |
| 32273002 | Immune thrombocytopenic purpura |
| 323079008 | Thrombocytopenia due to sequestration |
| 323666000 | Anemia due to intrinsic red cell abnormality |
| 3239007 | Lymphocyte disorder |
| 32648007 | Mild hereditary spherocytosis due to spectrin deficiency |
| 3272007 | Stomatocytosis |
| 328301000119102 | Pancytopenia due to antineoplastic chemotherapy |
| 32855007 | Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster |
| 32858009 | Hemolytic disease of fetus OR newborn due to ABO immunization |
| 32942005 | Glanzmann's thrombasthenia |
| 32984002 | Neonatal polycythemia |
| 33183004 | Post infectious thrombocytopenic purpura |
| 33491002 | Autoimmune hemolytic anemia caused by immunoglobulin A plus complement |
| 33905008 | Hereditary spherocytosis due to deficiency of protein 4.2 |
| 34194007 | Hereditary nonspherocytic hemolytic anemia due to pyrimidine-5'-nucleotidase deficiency |
| 34247008 | Anemia due to mechanical damage |
| 34395002 | Thrombocytopenia caused by hypothermia |
| 34397005 | Erythrocytosis due to uterine myoma |
| 34629009 | Anemia due to zinc deficiency |
| 34739009 | Urticaria pigmentosa, adult form |
| 34852006 | Glucose-6-phosphate dehydrogenase deficiency class II variant anemia |
| 34916006 | Neutrophil motility disorder |
| 34925000 | Megaloblastic anemia due to inborn errors of metabolism |
| 350353007 | De Vaal's syndrome |
| 350601000119109 | Hemolytic disease of newborn co-occurrent and due to ABO immunization |
| 350611000119107 | Hemolytic disease of fetus due to ABO immunization |
| 351287008 | Reticular dysgenesis with congenital aleukocytosis |
| 35434009 | Sickle cell-hemoglobin C disease |
| 35703006 | Post-viral paroxysmal cold hemoglobinuria |
| 3571004 | Megaloblastic anemia due to pancreatic insufficiency |
| 35778001 | Megaloblastic anemia due to error of folate metabolism |
| 359531004 | Amegakaryocytic thrombocytopenia with congenital malformation |
| 359536009 | Megakaryocytic aplasia |
| 360495000 | Familial megaloblastic anemia |
| 36070007 | Wiskott-Aldrich syndrome |
| 363041004 | Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism |
| 36467003 | Alpha plus thalassemia |
| 36472007 | Sickle cell-thalassemia disease |
| 36568005 | Hemolytic uremic syndrome of childhood |
| 36617002 | Immediate hemolytic transfusion reaction |
| 367328005 | Secondary polycythemia with excess erythropoietin |
| 367542003 | Pulmonary eosinophilia |
| 36874002 | Stress polycythemia |
| 36919001 | Anemia caused by lead |
| 370474006 | Eosinophilic myositis |
| 371046004 | Traumatic hemolytic anemia |
| 371074009 | Radiation thrombocytopenia |
| 371106008 | Idiopathic maternal thrombocytopenia |
| 371315009 | Iron deficiency anemia secondary to inadequate dietary iron intake |
| 37272000 | Rh deficiency syndrome |
| 373420004 | Upshaw-Schulman syndrome |
| 373421000 | Diarrhea-associated hemolytic uremic syndrome |
| 373422007 | Diarrhea-negative hemolytic uremic syndrome |
| 37370005 | Megaloblastic anemia caused by drugs |
| 37465004 | Plasmacytosis |
| 37492005 | Sex-linked thrombocytopenia |
| 38064006 | Reactive monocytosis |
| 38292009 | Red blood cell disorder |
| 38589006 | Mixed hemoglobin disorder |
| 38689004 | Hemolytic anemia due to infection |
| 38697006 | Polycythemia due to donor twin transfusion |
| 387702001 | Perinatal anemia |
| 387705004 | Hemolytic disease of fetus OR newborn due to isoimmunization |
| 387744007 | March hemoglobinuria |
| 387745008 | Sports anemia |
| 387759001 | Chronic granulomatous disease |
| 38911009 | Hereditary hemolytic anemia |
| 389147003 | Relative polycythemia |
| 389148008 | Pseudo-polycythemia |
| 389214003 | Diaphyseal dysplasia with anemia |
| 38959009 | Methemoglobinemia |
| 38970002 | Doan-Wright syndrome |
| 3902000 | Non dose-related drug-induced neutropenia |
| 3947004 | High oxygen affinity hemoglobin polycythemia |
| 39586009 | Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia |
| 397007003 | Mast cell disorder |
| 397008008 | Aggressive lymphadenopathic mastocytosis with eosinophilia |
| 397012002 | Cutaneous mastocytosis |
| 397013007 | Solitary cutaneous mastocytoma |
| 397014001 | Diffuse erythrodermic mastocytosis |
| 397015000 | Systemic mastocytosis with associated clonal hematological non-mast cell lineage disease |
| 397016004 | Systemic mast cell disease |
| 39778006 | Hemolytic transfusion reaction |
| 3978000 | Warm autoimmune hemolytic anemia |
| 398250003 | Familial hemophagocytic lymphohistiocytosis |
| 398623004 | Refractory anemia with excess blasts |
| 398937006 | Cold autoimmune hemolytic anemia |
| 40108008 | Thalassemia |
| 40145002 | Congenital neutrophil actin dysfunction |
| 40197009 | Chronic granulomatous disease, type IA |
| 402404006 | Episodic angioedema with eosinophilia |
| 402653004 | Thrombocytopenic purpura due to defective platelet production |
| 402654005 | Thrombocytopenic purpura due to platelet consumption |
| 402793008 | Heritable disorder of neutrophil production |
| 402794002 | Heritable disorder of neutrophil function |
| 403735006 | Eosinophilia-myalgia syndrome from tryptophan |
| 403837005 | Wiskott-Aldrich autosomal dominant variant syndrome |
| 403838000 | Jung syndrome |
| 403839008 | Siccardi syndrome |
| 40387008 | Polyagglutinable erythrocyte syndrome |
| 404170009 | Bullous urticaria pigmentosa |
| 404173006 | Familial mastocytosis |
| 406565005 | CD4 T lymphocyte deficiency |
| 406593009 | Methemoglobinemia caused by nitrate poisoning |
| 40679002 | Erythrocytosis due to alveolar hypoventilation |
| 409089005 | Febrile neutropenia |
| 413532003 | Anemia due to blood loss |
| 413533008 | Anemia due to chronic blood loss |
| 413565006 | Aplastic anemia associated with metabolic alteration |
| 413566007 | Aplastic anemia associated with pancreatitis |
| 413567003 | Aplastic anemia associated with pregnancy |
| 413603009 | Autoimmune hemolytic anemia |
| 41387000 | Hereditary nonspherocytic hemolytic anemia due to phosphofructokinase deficiency |
| 414022008 | Disorder of cellular component of blood |
| 414023003 | Disorder of cellular component of blood in newborn |
| 414127000 | Erythrocytosis due to polycythemia vera |
| 414393003 | Hereditary disorder of cellular element of blood |
| 414394009 | Hereditary red blood cell disorder |
| 414395005 | Hereditary white blood cell disorder |
| 41461004 | Platelet dysfunction caused by drugs |
| 41462006 | Anemia due to disturbance of proliferation AND/OR differentiation of erythroid precursor cells |
| 414850009 | Neutrophilia |
| 415005004 | Panleukopenia |
| 415283002 | Refractory anemia with excess blasts-1 |
| 415284008 | Refractory anemia with excess blasts-2 |
| 41614006 | Hypoplastic anemia |
| 416180004 | Hemoglobin SS disease without crisis |
| 416214006 | Sickle cell-hemoglobin D disease without crisis |
| 416290001 | Hemoglobin S sickling disorder without crisis |
| 416417002 | Hereditary hemoglobin S |
| 416484003 | Sickle cell-hemoglobin E disease with crisis |
| 416638004 | Sickle cell-hemoglobin E disease without crisis |
| 416729007 | Neutropenia associated with acquired immunodeficiency syndrome |
| 416826005 | Sickle cell-thalassemia disease with crisis |
| 416902009 | Uremic thrombocytopenia |
| 417048006 | Sickle cell-thalassemia disease without crisis |
| 417279003 | Hemoglobin S sickling disorder with crisis |
| 417357006 | Sickling disorder due to hemoglobin S |
| 417389002 | Disorder of basophils |
| 417425009 | Hemoglobin SS disease with crisis |
| 417517009 | Sickle cell-hemoglobin C disease with crisis |
| 417626001 | Thrombocytopenic purpura associated with metabolic disorder |
| 417672002 | Granulocytopenic disorder |
| 417683006 | Sickle cell-hemoglobin C disease without crisis |
| 417748003 | Sickle cell-hemoglobin D disease with crisis |
| 417967008 | Disorder of eosinophil |
| 41814009 | Neutropenia with dysgranulopoiesis |
| 41841004 | Sideroblastic anemia |
| 419455006 | Disorder characterized by eosinophilia |
| 420543008 | Anemia associated with acquired immunodeficiency syndrome |
| 421102007 | Aplastic anemia associated with acquired immunodeficiency syndrome |
| 421132004 | Platelet dysfunction associated with uremia |
| 421312009 | Agranulocytosis associated with acquired immunodeficiency syndrome |
| 421766003 | Thrombocytopenia associated with acquired immunodeficiency syndrome |
| 421851008 | Acquired hemolytic anemia associated with acquired immunodeficiency syndrome |
| 422167001 | Mycoplasmal anemia |
| 423486005 | Disseminated eosinophilic collagen disease |
| 42461002 | Anemia caused by copper |
| 42484009 | Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency |
| 424988008 | Anemia caused by substance |
| 42601008 | Congenital hemolytic anemia |
| 42616006 | Erythrocytosis due to hepatoma |
| 426800001 | Febrile granulocytopenia |
| 427245000 | Febrile leukopenia |
| 427306008 | Hereditary hemoglobinopathy |
| 428383000 | Anemia caused by medication |
| 42852008 | Infectious lymphocytosis |
| 430478003 | Macrophage activation syndrome |
| 430822009 | Basophilic leukemoid reaction |
| 43346008 | Platelet procoagulant activity deficiency |
| 43355006 | Eosinopenia |
| 43707008 | Anemia caused by heat |
| 438476003 | Autoimmune thrombotic thrombocytopenic purpura |
| 438492008 | Hereditary thrombocytopenic disorder |
| 43858000 | Secondary aplastic anemia |
| 439007008 | Acquired thrombotic thrombocytopenic purpura |
| 43918003 | Erythrocytosis due to renal tumor |
| 440206000 | Hemoglobin SS disease with vasoocclusive crisis |
| 441134009 | Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type |
| 441322009 | Drug induced thrombotic thrombocytopenic purpura |
| 44206008 | Hapten type low affinity hemolytic anemia |
| 44288006 | Anemia due to abnormality extrinsic to the red cell |
| 44306006 | T lymphocyte disorder |
| 444108000 | Acute sickle cell splenic sequestration crisis |
| 44452003 | Normocytic hypochromic anemia |
| 44456000 | Inappropriate secondary erythrocytosis |
| 444976001 | Congenital hemolytic uremic syndrome |
| 445542007 | Hemoglobin O-Arab trait |
| 44641000 | Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency |
| 44666001 | Microcytic hypochromic anemia |
| 447117006 | Hemoglobin H constant spring thalassemia |
| 44865000 | Secondary polycythemia |
| 44910003 | Megaloblastic anemia due to decreased intake of vitamin B>12< |
| 449784008 | Diffuse infiltrative lymphocytosis syndrome |
| 44992005 | Failed attempted abortion with intravascular hemolysis |
| 45098004 | Anemia due to multiple mechanisms |
| 45828008 | Anemia in mother complicating pregnancy, childbirth AND/OR puerperium |
| 462166006 | Fetal anemia |
| 46248003 | Hemoglobin E trait |
| 46359005 | Neutropenia associated with infectious disease |
| 46737006 | Normocytic normochromic anemia |
| 46760003 | Estren-Dameshek anemia |
| 47024008 | Sickle cell-hemoglobin E disease |
| 47047009 | Thalassemia with other hemoglobinopathy |
| 47084006 | beta^+^ Thalassemia, normal Hb A>2<, type 1, silent |
| 47100003 | Anemia of prematurity |
| 47144000 | Acute neutrophilia |
| 47318007 | Drug-induced neutropenia |
| 47516005 | Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin |
| 47526003 | Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency |
| 47844003 | Megaloblastic anemia due to chronic hemolytic anemia |
| 47986005 | Genetic anomaly of leukocyte |
| 48250002 | Gaisbock's syndrome |
| 48516007 | Acute infectious lymphocytosis |
| 4854004 | Acquired hemolytic anemia |
| 48553001 | Hemoglobin H disease |
| 48580008 | Anemia due to starvation |
| 48788004 | Cyclic thrombocytopenia |
| 48813009 | Lymphocytopenia |
| 48983004 | X chromosome-linked sideroblastic anemia |
| 49227001 | Phosphatidylcholine-sterol acyltransferase deficiency |
| 49284006 | Juvenile type megaloblastic anemia |
| 4939006 | Hemolytic anemia due to nonlymphoid neoplasm |
| 49472006 | Megaloblastic anemia due to vitamin B>12< deficiency |
| 49708008 | Anemia of chronic renal failure |
| 4984008 | Microcytic normochromic anemia |
| 49886003 | Thrombocytopenia due to blood loss |
| 50220002 | Cellular immunologic aplastic anemia |
| 50253007 | Secondary paroxysmal cold hemoglobinuria |
| 50715003 | Pure red cell aplasia |
| 50926003 | Job's syndrome |
| 51053007 | Hemoglobin C disease |
| 51071000 | Microangiopathic hemolytic anemia |
| 51448009 | Platelet secretory disorder |
| 51624005 | Dilutional thrombocytopenia |
| 51667002 | Anemia due to riboflavin deficiency |
| 51720005 | Gray platelet syndrome |
| 52212006 | Hereditary nonspherocytic hemolytic anemia due to glutathione reductase deficiency |
| 52413004 | Hereditary nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency |
| 52565000 | Non megaloblastic anemia associated with nutritional deficiency |
| 52951008 | Congenital dyserythropoietic anemia |
| 5300004 | Hemoglobin Bart's hydrops syndrome |
| 5315003 | Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity |
| 53165003 | Megaloblastic anemia |
| 53743006 | Anemia following fetal blood loss |
| 54006005 | Hereditary persistence of fetal hemoglobin delta beta plus thalassemia |
| 54097007 | White blood cell disorder |
| 5430006 | Megaloblastic anemia due to total parenteral nutrition |
| 54569005 | Bernard Soulier syndrome |
| 54698001 | Megaloblastic anemia due to Zollinger-Ellison syndrome |
| 55444004 | Transient neonatal neutropenia |
| 55907008 | Acquired aplastic anemia |
| 55995005 | Hereditary spherocytosis |
| 5603006 | Autoimmune hemolytic anemia caused by immunoglobulin G |
| 56205004 | Hereditary persistence of fetal hemoglobin, nondeletion type |
| 56478004 | Leukemoid reaction |
| 56918001 | Dose-related drug-induced neutropenia |
| 57020009 | Stokvis' disease |
| 57192008 | Acute pure red cell aplasia |
| 5876000 | Acquired pancytopenia |
| 59106005 | Anemia due to decreased red cell production |
| 59548005 | Congenital dyserythropoietic anemia, type I |
| 59644002 | Hereditary nonspherocytic hemolytic anemia due to phosphoglycerate kinase deficiency |
| 5967006 | A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis |
| 5994005 | Hereditary elliptocytosis due to deficiency of protein 4.1 |
| 60138009 | Anemia of pituitary deficiency |
| 60164003 | Megaloblastic anemia due to blind loop syndrome |
| 60504009 | Megaloblastic anemia due to congenital deficiency of intrinsic factor |
| 60628003 | Mediterranean macrothrombocytopenia |
| 60805002 | Hemolytic anemia with emphysema AND cutis laxa |
| 61261009 | Hemolytic anemia |
| 61395005 | Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia |
| 61744005 | Neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia |
| 61777009 | Thalassemia-hemoglobin C disease |
| 62074008 | Delta zero thalassemia |
| 62268000 | Hereditary nonspherocytic hemolytic anemia due to diphosphoglycerate mutase deficiency |
| 62389006 | Acute megaloblastic anemia due to severe illness |
| 62403005 | Glucose-6-phosphate dehydrogenase deficiency anemia |
| 62609001 | Autoimmune hemolytic anemia caused by immunoglobulin G plus complement |
| 62621000119107 | Fetal hemoglobinopathy |
| 62871001 | Idiopathic paroxysmal cold hemoglobinuria |
| 63175003 | Localized extracutaneous mastocytosis |
| 63444004 | Thrombocytopenia due to hypersplenism |
| 63484008 | Drug-induced neutrophilia |
| 63565007 | Congenital anemia |
| 6398009 | Idiopathic chronic cold agglutinin disease |
| 64249002 | Allergic eosinophilia |
| 64936001 | Löffler's syndrome |
| 65623009 | Immune neutropenia |
| 65959000 | Beta thalassemia |
| 66055002 | Alpha zero thalassemia |
| 66262001 | Hereditary elliptocytosis due to beta spectrin-ankyrin interaction |
| 66309005 | Antibody-mediated anemia |
| 6631009 | Thrombocytosis |
| 6659005 | Megaloblastic anemia due to nontropical sprue |
| 66612000 | Nutritional anemia |
| 66729008 | Hemoglobin D disease |
| 67023009 | Lymphocytosis |
| 67894009 | Megaloblastic anemia due to increased requirements |
| 68361004 | Late anemia due to isoimmunization |
| 68700003 | Megaloblastic anemia due to error of cobalamin metabolism |
| 68712004 | Lymphocytic hypoplasia |
| 68870007 | Congenital dyserythropoietic anemia, type II |
| 68913001 | Alpha thalassemia |
| 691381000119104 | Anemia due to chronic kidney disease stage 1 |
| 691401000119104 | Anemia co-occurrent and due to chronic kidney disease stage 4 |
| 691411000119101 | Anemia co-occurrent and due to chronic kidney disease stage 5 |
| 691421000119108 | Anemia co-occurrent and due to chronic kidney disease stage 3 |
| 69216008 | Hb Lepore thalassemia |
| 69574002 | Anemia of parathyroid dysfunction |
| 699208000 | Thrombocytopenia caused by alcohol |
| 69981004 | Hereditary spherocytosis due to beta spectrin defect |
| 703135009 | Anemia in malignant neoplastic disease |
| 70349007 | Pseudoneutrophilia |
| 703540008 | Chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia and neutrophilic dermatosis |
| 707323002 | Anemia co-occurrent and due to chronic kidney disease |
| 707324008 | Anemia co-occurrent and due to end stage renal disease |
| 707480001 | Chronic hemolytic anemia |
| 709465004 | Periodontitis co-occurrent with Chédiak-Higashi syndrome |
| 709535007 | Periodontitis co-occurrent with infantile genetic agranulocytosis |
| 70958007 | Plasma cell hyperplasia of bone marrow |
| 709608008 | Periodontitis co-occurrent with acquired neutropenia |
| 710735009 | Periodontitis co-occurrent with leukocyte adhesion deficiency |
| 710926008 | Periodontitis co-occurrent with familial neutropenia |
| 710927004 | Periodontitis co-occurrent with cyclical neutropenia |
| 711160007 | Eosinophil peroxidase deficiency |
| 711161006 | Hypochromic microcytic anemia with iron overload |
| 711407000 | Thrombocytopathy, asplenia and miosis |
| 712922002 | Myosin heavy chain 9 non muscle related disease |
| 713349004 | Anemia co-occurrent with human immunodeficiency virus infection |
| 713388002 | GATA binding protein 1 related thrombocytopenia with dyserythropoiesis |
| 713444005 | Hemophagocytic syndrome co-occurrent with human immunodeficiency virus infection |
| 713496008 | Anemia caused by zidovudine |
| 713508003 | Aplastic anemia co-occurrent with human immunodeficiency virus infection |
| 713530002 | Agranulocytosis co-occurrent with human immunodeficiency virus infection |
| 713533000 | Acquired hemolytic anemia co-occurrent with human immunodeficiency virus infection |
| 713694002 | Disorder of cellular component of blood caused by antiretroviral drug |
| 713910008 | Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent |
| 71436005 | Lazy leukocyte syndrome |
| 715342005 | Alpha thalassemia X-linked intellectual disability syndrome |
| 715526002 | Dehydrated hereditary stomatocytosis |
| 71610005 | Neutrophilic leukemoid reaction |
| 716192009 | Short stature and deafness with neutrophil dysfunction and facial dysmorphism syndrome |
| 716336002 | Congenital amegakaryocytic thrombocytopenia |
| 716655008 | Aggressive systemic mastocytosis |
| 716682000 | Dominant beta-thalassemia |
| 71692003 | Leukoerythroblastotic reaction |
| 717050005 | Autosomal recessive sideroblastic anemia |
| 71716005 | Erythrocytosis due to renal cyst |
| 717254007 | Familial pseudohyperkalemia |
| 717769007 | MYH9 macrothrombocytopenia syndrome |
| 717780007 | Monoclonal B-cell lymphocytosis |
| 717946000 | Megaloblastic anemia due to vitamin B12 deficiency secondary to intestinal disease |
| 717947009 | Vitamin B12 deficiency anemia caused by drug |
| 717948004 | Acquired iron deficiency anemia due to increased iron requirement |
| 718196002 | Beta thalassemia X-linked thrombocytopenia syndrome |
| 71832003 | Autoimmune hemolytic anemia caused by immunoglobulin M |
| 71855000 | Acute megaloblastic anemia secondary to total parenteral nutrition |
| 718553004 | White platelet syndrome |
| 718554005 | Medich giant platelet syndrome |
| 718614004 | Telangiectasia, erythrocytosis, monoclonal gammopathy, perinephric fluid collections and intrapulmonary shunting syndrome |
| 718716008 | Autoimmune hemolytic anemia mixed type |
| 718882006 | X-linked severe congenital neutropenia |
| 719019000 | WT limb blood syndrome |
| 719021005 | DK phocomelia syndrome |
| 719156006 | X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome |
| 719402008 | Lethal hemolytic anemia and genital anomaly syndrome |
| 719453009 | Congenital dyserythropoietic anemia type IV |
| 719816006 | X-linked sideroblastic anemia with spinocerebellar ataxia |
| 720401009 | Cystic fibrosis with gastritis and megaloblastic anemia syndrome |
| 720465002 | Adult-onset autosomal recessive sideroblastic anemia |
| 720520009 | Attenuated Chédiak-Higashi syndrome |
| 720521008 | Autosomal dominant macrothrombocytopenia |
| 720950009 | Familial thrombocytosis |
| 720982007 | Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome |
| 721184003 | Megaloblastic anemia due to folate deficiency due to increased requirement |
| 721185002 | Megaloblastic anemia due to folate deficiency in pregnancy and lactation |
| 721186001 | Megaloblastic anemia due to folate deficiency in prematurity |
| 721228006 | Huntington disease-like 2 |
| 721295000 | Acquired thiamine deficiency anemia |
| 721304007 | Refractory thrombocytopenia |
| 721882001 | Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome |
| 722005000 | Iron-refractory iron deficiency anemia |
| 722067005 | Severe combined immunodeficiency with hypereosinophilia |
| 722125003 | Overhydrated hereditary stomatocytosis |
| 722207000 | Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome |
| 722401001 | Severe fever with thrombocytopenia syndrome virus |
| 722453009 | Cutaneous mastocytosis, short stature, hearing loss syndrome |
| 722475006 | X-linked congenital dyserythropoietic anemia with thrombocytopenia |
| 722585009 | Polycythemia neonatorum due to inherited disorder of erythropoietin production |
| 722586005 | Polycythemia neonatorum following blood transfusion |
| 72272002 | Non malignant mast cell disease |
| 722721004 | Familial hemolytic uremic syndrome |
| 722925004 | Transient neonatal neutropenia due to congenital viral infection |
| 722926003 | Transient neonatal neutropenia due to neonatal bacterial sepsis |
| 72321000119107 | Sickle cell trait in mother complicating pregnancy |
| 72331000119105 | Thalassemia in mother complicating pregnancy |
| 723443003 | Neutrophil immunodeficiency syndrome |
| 723512008 | Revesz syndrome |
| 723623002 | Southeast Asian ovalocytosis |
| 724138007 | Mitochondrial myopathy with sideroblastic anemia syndrome |
| 724172004 | McLeod neuroacanthocytosis syndrome |
| 724556004 | Iron deficiency anemia due to blood loss |
| 724557008 | Acquired iron deficiency anemia due to decreased absorption |
| 724637001 | Isolated thrombocytopenia |
| 72501006 | Anemia caused by arsenic hydride |
| 725034002 | Familial platelet syndrome with predisposition to acute myelogenous leukemia |
| 725057008 | Nonspherocytic hemolytic anemia due to deficiency of adenosinetriphosphatase |
| 725105006 | Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor I |
| 725137007 | Neutropenia, monocytopenia, deafness syndrome |
| 725291001 | Defect of purinergic receptor p2y G protein-coupled 12 |
| 725463007 | Severe congenital hypochromic anemia with ringed sideroblasts |
| 726669007 | Central nervous system calcification, deafness, tubular acidosis, anemia syndrome |
| 73073009 | Hereditary elliptocytosis due to beta spectrin defect in self-association |
| 73162004 | Posttransfusion purpura |
| 73190000 | epsilon gamma delta beta^0^ Thalassemia |
| 732960002 | Secondary autoimmune hemolytic anemia co-occurrent and due to systemic lupus erythematosus |
| 732962005 | Secondary autoimmune hemolytic anemia co-occurrent and due to chronic inflammatory disease |
| 732963000 | Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder |
| 732965007 | Secondary autoimmune hemolytic anemia co-occurrent and due to rheumatic disorder |
| 732966008 | Secondary autoimmune hemolytic anemia co-occurrent and due to ulcerative colitis |
| 733064004 | Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome |
| 733096007 | Thyrocerebrorenal syndrome |
| 73397007 | Heparin-induced thrombocytopenia |
| 734349003 | Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 |
| 735434003 | Acquired neutrophilia |
| 735435002 | Constitutional neutrophilia |
| 735436001 | Acquired disorder of neutrophil function |
| 735437005 | Disorder of neutrophil adhesion |
| 735438000 | Disorder of neutrophil chemotaxis |
| 735439008 | Constitutional eosinopenia |
| 735440005 | Acquired eosinopenia |
| 735442002 | Acquired eosinophilia |
| 735443007 | Acquired lymphocytopenia |
| 735444001 | Acquired lymphocytosis |
| 735452003 | Hereditary vitamin B12 deficiency anemia |
| 735453008 | Hereditary folate deficiency anemia |
| 735748002 | Neonatal hemolysis co-occurrent and due to systemic bacterial infection |
| 736024007 | Pancytopenia caused by medication |
| 737209002 | Neonatal polycythemia due to placental insufficiency |
| 737210007 | Neonatal polycythemia due to intra-uterine growth retardation |
| 737220002 | Anemia due to metabolic disorder |
| 737221003 | Congenital thrombocytopenia |
| 73891003 | Acute megaloblastic anemia caused by nitrous oxide |
| 7391009 | Hemoglobin D trait |
| 74576004 | Acquired thrombocytopenia |
| 74703006 | Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency |
| 74789008 | Coombs positive hemolytic anemia |
| 74912001 | Hereditary methemoglobinemia due to globin chain mutation |
| 75063005 | Hemoglobinopathy with erythrocytosis |
| 75331009 | Evans syndrome |
| 75443009 | Hereditary elliptocytosis due to abnormal protein 4.1 |
| 75451007 | Thalassemia major |
| 76050008 | Hemoglobin C trait |
| 76243000 | Chronic granulomatous disease, type IVA |
| 76336008 | Delta beta zero thalassemia |
| 76366001 | Hemolytic anemia caused by Bartonella |
| 763713000 | Idiopathic CD4 lymphocytopenia |
| 763864008 | Persistent polyclonal B-cell lymphocytosis |
| 765327005 | Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome |
| 765748009 | Adult pure red cell aplasia |
| 765977002 | Bleeding disorder due to glycoprotein VI deficiency |
| 76621000 | Urticaria pigmentosa, infantile form |
| 766982000 | Hemolytic anemia due to adenylate kinase deficiency |
| 767497003 | Autosomal recessive congenital methemoglobinemia |
| 767498008 | Autosomal recessive congenital methemoglobinemia type II |
| 767499000 | Autosomal recessive congenital methemoglobinemia type I |
| 76762001 | Eosinophilic myopathy |
| 767657005 | Anemia due to and following chemotherapy |
| 767658000 | Neutropenia due to and following chemotherapy |
| 768556005 | Ataxia pancytopenia syndrome |
| 76873001 | Polycythemia due to maternal-fetal transfusion |
| 769167005 | Vaso-occlusive pain co-occurrent and due to sickle cell disease |
| 770402000 | Aleukemic mast cell leukemia |
| 770407006 | Chuvash erythrocytosis |
| 77084001 | Immunologic aplastic anemia |
| 770942003 | Kostmann syndrome |
| 770947009 | Autosomal dominant severe congenital neutropenia |
| 771075004 | Macrothrombocytopenia with mitral valve insufficiency |
| 771511005 | Thrombocythemia with distal limb defect |
| 772126000 | Poikiloderma with neutropenia |
| 77330006 | Chronic granulomatous disease, type II |
| 773489008 | Hereditary cryohydrocytosis with normal stomatin |
| 77358003 | Congenital leukocyte adherence deficiency |
| 774071007 | Pancytopenia with developmental delay syndrome |
| 774083009 | Neonatal autoimmune hemolytic anemia |
| 77413008 | Severe hereditary spherocytosis due to spectrin deficiency |
| 775909002 | Congenital neutropenia, myelofibrosis, nephromegaly syndrome |
| 77607006 | Drug-induced sideroblastic anemia |
| 77663007 | Hemolytic anemia caused by malaria |
| 778024005 | Monocytopenia with susceptibility to infections |
| 778027003 | Primary CD59 deficiency |
| 778050009 | Idiopathic eosinophilic myositis |
| 78129009 | Thrombotic thrombocytopenic purpura |
| 78209002 | Hemolytic uremic syndrome, adult type |
| 782759001 | X-linked dyserythropoietic anemia with abnormal platelets and neutropenia |
| 782866008 | Eosinophilic peritonitis |
| 782880001 | Hemoglobinopathy Toms River |
| 782911008 | Hereditary cryohydrocytosis with reduced stomatin |
| 782915004 | Acquired hemophagocytic lymphohistiocytosis associated with malignant disease |
| 782934004 | Bleeding diathesis due to collagen receptor defect |
| 783058007 | Autosomal recessive severe congenital neutropenia due to glucose-6-phosphatase catalytic subunit 3 deficiency |
| 783142006 | Pancytopenia due to IKAROS family zinc finger 1 mutations |
| 783194008 | Bleeding diathesis due to thromboxane synthesis deficiency |
| 783199003 | Autosomal recessive severe congenital neutropenia due to jagunal homolog 1 deficiency |
| 783200000 | Autosomal recessive severe congenital neutropenia due to C-X-C motif chemokine receptor 2 deficiency |
| 783201001 | Autosomal recessive severe congenital neutropenia due to colony stimulating factor 3 receptor deficiency |
| 783202008 | Autosomal dominant secondary polycythemia |
| 783211008 | Non-chronic lymphocytic leukemia monoclonal B-cell lymphocytosis |
| 783251006 | Hereditary thrombocytopenia with normal platelets |
| 783254003 | Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome |
| 783255002 | Hereditary isolated aplastic anemia |
| 78345002 | Thrombocytopenia due to diminished platelet production |
| 783766005 | Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene |
| 78378009 | Isoimmune neutropenia |
| 784392009 | Adult chronic idiopathic neutropenia |
| 78578005 | Erythrocytosis due to pulmonary disease |
| 78677008 | Anemia due to pantothenic deficiency |
| 786855003 | Monoclonal B-cell lymphocytosis chronic lymphocytic leukemia-type |
| 78745000 | Urticaria pigmentosa |
| 788865000 | Anemia due to chronic infectious disease |
| 788944005 | Gamma delta beta thalassemia |
| 78908001 | Hereditary nonspherocytic hemolytic anemia due to decreased adenosine deaminase activity |
| 789660001 | Atypical hemolytic uremic syndrome |
| 789697006 | Mast cell gastritis |
| 78997000 | Megaloblastic anemia due to vegetarianism |
| 79035003 | Anemia due to unknown mechanism |
| 7933002 | Neonatal thrombocytopenia associated with maternal idiopathic thrombocytopenic purpura |
| 79336007 | Familial eosinophilia |
| 79592006 | Beta plus thalassemia |
| 80126007 | Plummer-Vinson syndrome |
| 80141007 | Hemoglobinopathy |
| 80255009 | Maternal transfer neutropenia |
| 80369006 | Chronic neutrophilia |
| 80511004 | Erythrocytosis due to endocrine disorder |
| 80875006 | Achlorhydric anemia |
| 80963002 | Glucose-6-phosphate dehydrogenase deficiency class V variant anemia |
| 81711008 | Hemolytic anemia caused by drugs |
| 82003006 | Glucose-6-phosphate dehydrogenase deficiency class IV variant anemia |
| 8214000 | Telangiectasia macularis eruptiva perstans |
| 82190001 | Thrombocytopenia due to defective platelet production |
| 82317007 | Chronic granulomatous disease, type III |
| 82430007 | Acute megaloblastic anemia |
| 82546001 | Reactive immunoproliferative disease |
| 82835005 | Neonatal thrombocytopenia |
| 82895008 | Megaloblastic anemia due to disease of small intestine |
| 82980005 | Anemia due to diabetes mellitus |
| 83250000 | Delayed hemolytic transfusion reaction |
| 83414005 | Macrocytic anemia |
| 84027009 | Pernicious anemia |
| 840505007 | Down syndrome co-occurrent with leukemoid reaction associated transient neonatal pustulosis |
| 84188003 | Thalassemia syndrome |
| 84260001 | Hemoglobinopathy with cyanosis |
| 84828003 | Leukopenia |
| 85422000 | alpha^+^ Thalassemia, nondeletion type |
| 85557000 | Hereditary persistence of fetal hemoglobin deletion type |
| 85559002 | Pelger-Huët anomaly |
| 85570009 | Anemia due to vitamin A deficiency |
| 85589009 | Radial aplasia-thrombocytopenia syndrome |
| 85649008 | Megaloblastic anemia due to folate deficiency |
| 85746008 | Anemia due to protein deficiency |
| 860824009 | Eosinophilia due to infectious disease |
| 860827002 | Eosinopenia due to infectious disease |
| 862001 | Anemia caused by chlorate |
| 86225009 | Hapten type high affinity hemolytic anemia |
| 86242003 | alpha^+^ Thalassemia, deletion type |
| 86325007 | Non megaloblastic anemia due to alcoholism |
| 863953007 | Primaquine sensitivity anemia |
| 86448001 | Anemia due to vitamin B>6< deficiency |
| 866084002 | Lymphopenia due to infection |
| 866092006 | Megaloblastic anemia due to dihydrofolate reductase deficiency |
| 866151004 | Lymphocytopenia due to Severe acute respiratory syndrome coronavirus 2 |
| 866152006 | Thrombocytopenia due to Severe acute respiratory syndrome coronavirus 2 |
| 86635005 | Kasabach-Merritt syndrome |
| 866381000000109 | Recurrent anaemia |
| 866901000000103 | Eosinophilic bronchitis |
| 86715000 | Beta zero thalassemia |
| 86859003 | Glucose-6-phosphate dehydrogenase variant enzyme deficiency anemia |
| 86986002 | Hemolytic disease of fetus OR newborn due to RhD isoimmunization |
| 870431002 | Delayed hemolysis following artesunate therapy |
| 874900008 | Moderate deficiency of glucose-6-phosphate dehydrogenase |
| 87522002 | Iron deficiency anemia |
| 87806008 | Megaloblastic anemia due to tropical sprue |
| 87810006 | Megaloblastic anemia caused by alcoholism |
| 87902006 | Thrombocytopenia due to non-immune destruction |
| 87994004 | Xerocytosis |
| 8857001 | Hereditary elliptocytosis due to alpha spectrin defect |
| 88854002 | Congenital hypoplastic anemia |
| 89454001 | Shwachman syndrome |
| 89459006 | Hereditary persistence of fetal hemoglobin linked to beta-globulin gene cluster |
| 89655007 | Congenital neutropenia |
| 89810003 | ^A^gamma delta beta^0^ thalassemia |
| 89962000 | Neonatal thrombocytopenia due to exchange transfusion |
| 90175006 | Secondary acquired sideroblastic anemia |
| 90414007 | Chronic acquired pure red cell aplasia |
| 90501009 | Erythrocytosis due to defective oxygen transport |
| 91217009 | Megaloblastic anemia due to pregnancy |
| 91411007 | Autoimmune hemolytic anemia caused by immunoglobulin A |
| 9311003 | Hermansky-Pudlak syndrome |
| 934007 | Thalassemia intermedia |
| 9417000 | Platelet dense granule deficiency |
| 9426002 | Erythrocytosis due to hydronephrosis |
| 9434008 | Hereditary pyropoikilocytosis |
| 95416007 | Eosinophilia myalgia syndrome |
| 95557003 | Red blood cell sequestration in liver |
| 95605009 | Hemolysis-elevated liver enzymes-low platelet count syndrome |
| 95624007 | Neonatal lymphocytopenia |
| 95733001 | Eosinophilic keratitis |
| 97571000119109 | Thrombocytopenia co-occurrent and due to alcoholism |
| 9764001 | Anemia caused by radiation |