ICD-10 Diagnoses

More than 60,611 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	save
Constitutional (pure) red blood cell aplasia	D61.01	save
Other constitutional aplastic anemia	D61.09	save
Drug-induced aplastic anemia	D61.1	save
Aplastic anemia due to other external agents	D61.2	save
Idiopathic aplastic anemia	D61.3	save
Antineoplastic chemotherapy induced pancytopenia	D61.810	save
Other drug-induced pancytopenia	D61.811	save
Other pancytopenia	D61.818	save
Myelophthisis	D61.82	save
Other specified aplastic anemias and other bone marrow failure syndromes	D61.89	save
Aplastic anemia, unspecified	D61.9	save
Acute posthemorrhagic anemia	D62	save
Anemia in neoplastic disease	D63.0	save
Anemia in chronic kidney disease	D63.1	save
Anemia in other chronic diseases classified elsewhere	D63.8	save
Hereditary sideroblastic anemia	D64.0	save
Secondary sideroblastic anemia due to disease	D64.1	save
Secondary sideroblastic anemia due to drugs and toxins	D64.2	save
Other sideroblastic anemias	D64.3	save
Congenital dyserythropoietic anemia	D64.4	save
Anemia due to antineoplastic chemotherapy	D64.81	save
Other specified anemias	D64.89	save
Anemia, unspecified	D64.9	save
Disseminated intravascular coagulation [defibrination syndrome]	D65	save
Hereditary factor VIII deficiency	D66	save
Hereditary factor IX deficiency	D67	save
Von Willebrand's disease	D68.0	save
Von Willebrand disease, unspecified	D68.00	save
Von Willebrand disease, type 1	D68.01	save
Von Willebrand disease, type 2A	D68.020	save
Von Willebrand disease, type 2B	D68.021	save
Von Willebrand disease, type 2M	D68.022	save
Von Willebrand disease, type 2N	D68.023	save
Von Willebrand disease, type 2, unspecified	D68.029	save
Von Willebrand disease, type 3	D68.03	save
Acquired von Willebrand disease	D68.04	save
Other von Willebrand disease	D68.09	save
Hereditary factor XI deficiency	D68.1	save
Hereditary deficiency of other clotting factors	D68.2	save
Acquired hemophilia	D68.311	save
Antiphospholipid antibody with hemorrhagic disorder	D68.312	save
Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors	D68.318	save
Hemorrhagic disorder due to extrinsic circulating anticoagulants	D68.32	save
Acquired coagulation factor deficiency	D68.4	save
Activated protein C resistance	D68.51	save
Prothrombin gene mutation	D68.52	save
Other primary thrombophilia	D68.59	save
Antiphospholipid syndrome	D68.61	save
Lupus anticoagulant syndrome	D68.62	save

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