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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 |
|---|---|---|---|---|
| Fetofetal Transfusion Passage of blood from one fetus to another via an arteriovenous communication or other shunt, in a monozygotic twin pregnancy. It results in anemia i… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150034 |
| Fetomaternal Transfusion Transplacental passage of fetal blood into the circulation of the maternal organism. (Dorland, 27th ed) | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150035 |
| GATA2 Deficiency A rare disorder of the immune system with wide-ranging effects which include GATA2 Transcription Factor dysfunction, immunodeficiency, myelodysplasti… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150102 |
| Glucosephosphate Dehydrogenase Deficiency A disease-producing enzyme deficiency subject to many variants, some of which cause a deficiency of GLUCOSE-6-PHOSPHATE DEHYDROGENASE activity in ery… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150018 |
| Granuloma A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents. | Pathologic Condition | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150156 |
| Granulomatous Disease, Chronic A defect of leukocyte function in which phagocytic cells ingest but fail to digest bacteria, resulting in recurring bacterial infections with granulo… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150127 |
| Gray Platelet Syndrome A rare, inherited platelet disorder characterized by a selective deficiency in the number and contents of platelet alpha-granules. It is associated w… | Syndrome | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150076 |
| Heavy Chain Disease A disorder of immunoglobulin synthesis in which large quantities of abnormal heavy chains are excreted in the urine. The amino acid sequences of the … | Immune Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150095 |
| Hematologic Diseases Disorders of the blood and blood forming tissues. | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150002 |
| Hemic and Lymphatic Diseases Hematologic diseases and diseases of the lymphatic system collectively. Hemic diseases include disorders involving the formed elements (e.g., ERYTHRO… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150001 |
| Hemoglobin C Disease A disease characterized by compensated hemolysis with a normal hemoglobin level or a mild to moderate anemia. There may be intermittent abdominal dis… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150020 |
| Hemoglobin SC Disease One of the sickle cell disorders characterized by the presence of both hemoglobin S and hemoglobin C. It is similar to, but less severe than sickle c… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150014 |
| Hemoglobinopathies A group of inherited disorders characterized by structural alterations within the hemoglobin molecule. | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150116 |
| Hemoglobinuria, Paroxysmal A condition characterized by the recurrence of HEMOGLOBINURIA caused by intravascular HEMOLYSIS. In cases occurring upon cold exposure (paroxysmal co… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150026 |
| Hemophilia A The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tend… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150052 |
| Hemophilia B A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Christmas Disease, after the first patient studied in d… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150053 |
| Hemorrhagic Disorders Spontaneous or near spontaneous bleeding caused by a defect in clotting mechanisms (BLOOD COAGULATION DISORDERS) or another abnormality causing a str… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150117 |
| Histiocytic Necrotizing Lymphadenitis Development of lesions in the lymph node characterized by infiltration of the cortex or paracortex by large collections of proliferating histiocytes … | Inflammatory Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150142 |
| Histiocytosis General term for the abnormal appearance of histiocytes in the blood. Based on the pathological features of the cells involved rather than on clinica… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150135 |
| Histiocytosis, Non-Langerhans-Cell Group of disorders which feature accumulations of active HISTIOCYTES and LYMPHOCYTES, but where the histiocytes are not LANGERHANS CELLS. The group i… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150136 |
| Histiocytosis, Sinus Benign, non-Langerhans-cell, histiocytic proliferative disorder that primarily affects the lymph nodes. It is often referred to as sinus histiocytosi… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150138 |
| Hyper-IgM Immunodeficiency Syndrome A rare inherited immunodeficiency syndrome characterized by normal or elevated serum IMMUNOGLOBULIN M levels with absence of IMMUNOGLOBULIN G; IMMUNO… | Syndrome | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150086 |
| Hyper-IgM Immunodeficiency Syndrome, Type 1 An X-linked hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding CD40 LIGAND. | Syndrome | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150087 |
| Hypereosinophilic Syndrome A heterogeneous group of disorders with the common feature of prolonged eosinophilia of unknown cause and associated organ system dysfunction, includ… | Syndrome | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150121 |
| Hypergammaglobulinemia An excess of GAMMA-GLOBULINS in the serum due to chronic infections or PARAPROTEINEMIAS. | Immune Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150090 |
| Hypersplenism Condition characterized by splenomegaly, some reduction in the number of circulating blood cells in the presence of a normal or hyperactive bone marr… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150163 |
| Hypoalbuminemia A condition in which albumin level in blood (SERUM ALBUMIN) is below the normal range. Hypoalbuminemia may be due to decreased hepatic albumin synthe… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150093 |
| Hypoproteinemia A condition in which total serum protein level is below the normal range. Hypoproteinemia can be caused by protein malabsorption in the gastrointesti… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150092 |
| Hypoprothrombinemias Absence or reduced levels of PROTHROMBIN in the blood. | Vascular Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150054 |
| IgA Deficiency A dysgammaglobulinemia characterized by a deficiency of IMMUNOGLOBULIN A. | Immune Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150088 |