Code
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| Description
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|---|---|
D581
|
Hereditary elliptocytosis
|
D582
|
Other hemoglobinopathies
|
D588
|
Other specified hereditary hemolytic anemias
|
D589
|
Hereditary hemolytic anemia, unspecified
|
D590
|
Drug-induced autoimmune hemolytic anemia
|
D5910
|
Autoimmune hemolytic anemia, unspecified
|
D5911
|
Warm autoimmune hemolytic anemia
|
D5912
|
Cold autoimmune hemolytic anemia
|
D5913
|
Mixed type autoimmune hemolytic anemia
|
D5919
|
Other autoimmune hemolytic anemia
|
D592
|
Drug-induced nonautoimmune hemolytic anemia
|
D593
|
Hemolytic-uremic syndrome
|
D594
|
Other nonautoimmune hemolytic anemias
|
D595
|
Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]
|
D596
|
Hemoglobinuria due to hemolysis from other external causes
|
D598
|
Other acquired hemolytic anemias
|
D599
|
Acquired hemolytic anemia, unspecified
|
D600
|
Chronic acquired pure red cell aplasia
|
D601
|
Transient acquired pure red cell aplasia
|
D608
|
Other acquired pure red cell aplasias
|
D609
|
Acquired pure red cell aplasia, unspecified
|
D6101
|
Constitutional (pure) red blood cell aplasia
|
D6109
|
Other constitutional aplastic anemia
|
D611
|
Drug-induced aplastic anemia
|
D612
|
Aplastic anemia due to other external agents
|
D613
|
Idiopathic aplastic anemia
|
D61810
|
Antineoplastic chemotherapy induced pancytopenia
|
D61811
|
Other drug-induced pancytopenia
|
D61818
|
Other pancytopenia
|
D6182
|
Myelophthisis
|
D6189
|
Other specified aplastic anemias and other bone marrow failure syndromes
|
D619
|
Aplastic anemia, unspecified
|
D62
|
Acute posthemorrhagic anemia
|
D630
|
Anemia in neoplastic disease
|
D631
|
Anemia in chronic kidney disease
|
D638
|
Anemia in other chronic diseases classified elsewhere
|
D640
|
Hereditary sideroblastic anemia
|
D641
|
Secondary sideroblastic anemia due to disease
|
D642
|
Secondary sideroblastic anemia due to drugs and toxins
|
D643
|
Other sideroblastic anemias
|
D644
|
Congenital dyserythropoietic anemia
|
D6481
|
Anemia due to antineoplastic chemotherapy
|
D6489
|
Other specified anemias
|
D649
|
Anemia, unspecified
|
D65
|
Disseminated intravascular coagulation [defibrination syndrome]
|
D66
|
Hereditary factor VIII deficiency
|
D67
|
Hereditary factor IX deficiency
|
D680
|
Von Willebrand's disease
|
D681
|
Hereditary factor XI deficiency
|
D682
|
Hereditary deficiency of other clotting factors
|
D68311
|
Acquired hemophilia
|
D68312
|
Antiphospholipid antibody with hemorrhagic disorder
|
D68318
|
Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
|
D6832
|
Hemorrhagic disorder due to extrinsic circulating anticoagulants
|
D684
|
Acquired coagulation factor deficiency
|
D6851
|
Activated protein C resistance
|
D6852
|
Prothrombin gene mutation
|
D6859
|
Other primary thrombophilia
|
D6861
|
Antiphospholipid syndrome
|
D6862
|
Lupus anticoagulant syndrome
|
D6869
|
Other thrombophilia
|
D688
|
Other specified coagulation defects
|
D689
|
Coagulation defect, unspecified
|
D690
|
Allergic purpura
|
D691
|
Qualitative platelet defects
|
D692
|
Other nonthrombocytopenic purpura
|
D693
|
Immune thrombocytopenic purpura
|
D6941
|
Evans syndrome
|
D6942
|
Congenital and hereditary thrombocytopenia purpura
|
D6949
|
Other primary thrombocytopenia
|
D6951
|
Posttransfusion purpura
|
D6959
|
Other secondary thrombocytopenia
|
D696
|
Thrombocytopenia, unspecified
|
D698
|
Other specified hemorrhagic conditions
|
D699
|
Hemorrhagic condition, unspecified
|
D700
|
Congenital agranulocytosis
|
D701
|
Agranulocytosis secondary to cancer chemotherapy
|
D702
|
Other drug-induced agranulocytosis
|
D703
|
Neutropenia due to infection
|
D704
|
Cyclic neutropenia
|
D708
|
Other neutropenia
|
D709
|
Neutropenia, unspecified
|
D71
|
Functional disorders of polymorphonuclear neutrophils
|
D720
|
Genetic anomalies of leukocytes
|
D7210
|
Eosinophilia, unspecified
|
D72110
|
Idiopathic hypereosinophilic syndrome [IHES]
|
D72111
|
Lymphocytic Variant Hypereosinophilic Syndrome [LHES]
|
D72118
|
Other hypereosinophilic syndrome
|
D72119
|
Hypereosinophilic syndrome [HES], unspecified
|
D7212
|
Drug rash with eosinophilia and systemic symptoms syndrome
|
D7218
|
Eosinophilia in diseases classified elsewhere
|
D7219
|
Other eosinophilia
|
D72810
|
Lymphocytopenia
|
D72818
|
Other decreased white blood cell count
|
D72819
|
Decreased white blood cell count, unspecified
|
D72820
|
Lymphocytosis (symptomatic)
|
D72821
|
Monocytosis (symptomatic)
|
D72822
|
Plasmacytosis
|
D72823
|
Leukemoid reaction
|
D72824
|
Basophilia
|
Subsets and Splits
Diabetes Codes E10-E14
The query retrieves and sorts records with "Code" values between 'E10' and 'E14', offering a basic filter of the dataset but not providing significant analytical insights.