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ICD-10 Diagnoses

More than 60,609 Diagnosis Codes Covered

ICD-10 Diagnosis Codes are globally recognized labels for health conditions. At Disease.eXpert, we elucidate the medical information tied to these codes, offering clear and user-friendly explanations about the corresponding symptoms, treatments, and more.

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Diagnosis Codes List

Name ICD10
Action
Acquired pure red cell aplasia, unspecified D60.9
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Constitutional (pure) red blood cell aplasia D61.01
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Other constitutional aplastic anemia D61.09
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Drug-induced aplastic anemia D61.1
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Aplastic anemia due to other external agents D61.2
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Idiopathic aplastic anemia D61.3
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Antineoplastic chemotherapy induced pancytopenia D61.810
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Other drug-induced pancytopenia D61.811
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Other pancytopenia D61.818
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Myelophthisis D61.82
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Other specified aplastic anemias and other bone marrow failure syndromes D61.89
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Aplastic anemia, unspecified D61.9
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Acute posthemorrhagic anemia D62
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Anemia in neoplastic disease D63.0
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Anemia in chronic kidney disease D63.1
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Anemia in other chronic diseases classified elsewhere D63.8
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Hereditary sideroblastic anemia D64.0
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Secondary sideroblastic anemia due to disease D64.1
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Secondary sideroblastic anemia due to drugs and toxins D64.2
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Other sideroblastic anemias D64.3
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Congenital dyserythropoietic anemia D64.4
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Anemia due to antineoplastic chemotherapy D64.81
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Other specified anemias D64.89
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Anemia, unspecified D64.9
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Disseminated intravascular coagulation [defibrination syndrome] D65
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Hereditary factor VIII deficiency D66
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Hereditary factor IX deficiency D67
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Von Willebrand's disease D68.0
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Von Willebrand disease, unspecified D68.00
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Von Willebrand disease, type 1 D68.01
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Von Willebrand disease, type 2A D68.020
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Von Willebrand disease, type 2B D68.021
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Von Willebrand disease, type 2M D68.022
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Von Willebrand disease, type 2N D68.023
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Von Willebrand disease, type 2, unspecified D68.029
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Von Willebrand disease, type 3 D68.03
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Acquired von Willebrand disease D68.04
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Other von Willebrand disease D68.09
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Hereditary factor XI deficiency D68.1
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Hereditary deficiency of other clotting factors D68.2
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Acquired hemophilia D68.311
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Antiphospholipid antibody with hemorrhagic disorder D68.312
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Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors D68.318
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Hemorrhagic disorder due to extrinsic circulating anticoagulants D68.32
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Acquired coagulation factor deficiency D68.4
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Activated protein C resistance D68.51
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Prothrombin gene mutation D68.52
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Other primary thrombophilia D68.59
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Antiphospholipid syndrome D68.61
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Lupus anticoagulant syndrome D68.62
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Displaying Item 2951 - 3000 of 72921 in total