Diseases

Explore disease pages that summarize symptoms, diagnostic context, and related care topics.

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All diseases (73,990)

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

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

D6800

Von Willebrand disease, unspecified

D6801

Von Willebrand disease, type 1

D68020

Von Willebrand disease, type 2A

D68021

Von Willebrand disease, type 2B

D68022

Von Willebrand disease, type 2M

D68023

Von Willebrand disease, type 2N

D68029

Von Willebrand disease, type 2, unspecified

D6803

Von Willebrand disease, type 3

D6804

Acquired von Willebrand disease

D6809

Other von Willebrand 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

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

D711

Leukocyte adhesion deficiency

D718

Other functional disorders of polymorphonuclear neutrophils

D719

Functional disorders of polymorphonuclear neutrophils, unspecified

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

D72825

Bandemia

D72828

Other elevated white blood cell count

D72829

Elevated white blood cell count, unspecified

D7289

Other specified disorders of white blood cells

D729

Disorder of white blood cells, unspecified

D730

Hyposplenism

D731

Hypersplenism

D732

Chronic congestive splenomegaly

D733

Abscess of spleen

D734

Cyst of spleen

D735

Infarction of spleen

D7381

Neutropenic splenomegaly

D7389

Other diseases of spleen

D739

Disease of spleen, unspecified

D740

Congenital methemoglobinemia

D748

Other methemoglobinemias

D749

Methemoglobinemia, unspecified

D750

Familial erythrocytosis

D751

Secondary polycythemia

D7581

Myelofibrosis

D75821

Non-immune heparin-induced thrombocytopenia

D75828

Other heparin-induced thrombocytopenia syndrome

D75829

Heparin-induced thrombocytopenia, unspecified

D75838

Other thrombocytosis

D75839

Thrombocytosis, unspecified

D7584

Other platelet-activating anti-PF4 disorders

D7589

Other specified diseases of blood and blood-forming organs

D759

Disease of blood and blood-forming organs, unspecified

D75A

Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia

D761

Hemophagocytic lymphohistiocytosis

D762

Hemophagocytic syndrome, infection-associated

D763

Other histiocytosis syndromes