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Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Any direct membership
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| Activated Protein C Resistance A hemostatic disorder characterized by a poor anticoagulant response to activated protein C (APC). The activated form of Factor V (Factor Va) is more… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150042 |
| Afibrinogenemia A deficiency or absence of FIBRINOGEN in the blood. | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150043 |
| Agammaglobulinemia An immunologic deficiency state characterized by an extremely low level of generally all classes of gamma-globulin in the blood. | Immune Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150084 |
| Agranulocytosis A decrease in the number of GRANULOCYTES; (BASOPHILS; EOSINOPHILS; and NEUTROPHILS). | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150109 |
| alpha-Thalassemia A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, d… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150023 |
| Anemia A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN. | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150003 |
| Anemia, Aplastic A form of anemia in which the bone marrow fails to produce adequate numbers of peripheral blood elements. | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150004 |
| Anemia, Diamond-Blackfan A rare congenital hypoplastic anemia that usually presents early in infancy. The disease is characterized by a moderate to severe macrocytic anemia, … | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150006 |
| Anemia, Dyserythropoietic, Congenital A familial disorder characterized by ANEMIA with multinuclear ERYTHROBLASTS, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and vari… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150011 |
| Anemia, Hemolytic A condition of inadequate circulating red blood cells (ANEMIA) or insufficient HEMOGLOBIN due to premature destruction of red blood cells (ERYTHROCYT… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150008 |
| Anemia, Hemolytic, Autoimmune Acquired hemolytic anemia due to the presence of AUTOANTIBODIES which agglutinate or lyse the patient's own RED BLOOD CELLS. | Immune Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150009 |
| Anemia, Hemolytic, Congenital Hemolytic anemia due to various intrinsic defects of the erythrocyte. | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150010 |
| Anemia, Hemolytic, Congenital Nonspherocytic Any one of a group of congenital hemolytic anemias in which there is no abnormal hemoglobin or spherocytosis and in which there is a defect of glycol… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150012 |
| Anemia, Hypochromic Anemia characterized by a decrease in the ratio of the weight of hemoglobin to the volume of the erythrocyte, i.e., the mean corpuscular hemoglobin c… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150027 |
| Anemia, Hypoplastic, Congenital An inborn condition characterized by deficiencies of red cell precursors that sometimes also includes LEUKOPENIA and THROMBOCYTOPENIA. | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150005 |
| Anemia, Iron-Deficiency Anemia characterized by decreased or absent iron stores, low serum iron concentration, low transferrin saturation, and low hemoglobin concentration o… | Metabolic Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150028 |
| Anemia, Macrocytic Anemia characterized by larger than normal erythrocytes, increased mean corpuscular volume (MCV) and increased mean corpuscular hemoglobin (MCH). | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150029 |
| Anemia, Megaloblastic A disorder characterized by the presence of ANEMIA, abnormally large red blood cells (megalocytes or macrocytes), and MEGALOBLASTS. | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150030 |
| Anemia, Myelophthisic Anemia characterized by appearance of immature myeloid and nucleated erythrocytes in the peripheral blood, resulting from infiltration of the bone ma… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150032 |
| Anemia, Neonatal The mildest form of erythroblastosis fetalis in which anemia is the chief manifestation. | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150033 |
| Anemia, Pernicious A megaloblastic anemia occurring in children but more commonly in later life, characterized by histamine-fast achlorhydria, in which the laboratory a… | Metabolic Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150031 |
| Anemia, Refractory A severe sometimes chronic anemia, usually macrocytic in type, that does not respond to ordinary antianemic therapy. | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150036 |
| Anemia, Refractory, with Excess of Blasts Chronic refractory anemia with granulocytopenia, and/or thrombocytopenia. Myeloblasts and progranulocytes constitute 5 to 40 percent of the nucleated… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150037 |
| Anemia, Sickle Cell A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expressio… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150013 |
| Anemia, Sideroblastic Anemia characterized by the presence of erythroblasts containing excessive deposits of iron in the marrow. | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150038 |
| Angiolymphoid Hyperplasia with Eosinophilia Solitary or multiple benign cutaneous nodules comprised of immature and mature vascular structures intermingled with endothelial cells and a varied i… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150120 |
| Antithrombin III Deficiency An absence or reduced level of Antithrombin III leading to an increased risk for thrombosis. | Vascular Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150044 |
| Autoimmune Lymphoproliferative Syndrome Rare congenital lymphoid disorder due to mutations in certain Fas-Fas ligand pathway genes. Known causes include mutations in FAS, TNFSF6, NRAS, CASP… | Syndrome | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150154 |
| Bernard-Soulier Syndrome A familial coagulation disorder characterized by a prolonged bleeding time, unusually large platelets, and impaired prothrombin consumption. | Syndrome | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150045 |
| beta-Thalassemia A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous fo… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150024 |