Public registry
Nodes
Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Base domain only
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| Anastomotic Leak Breakdown of the connection and subsequent leakage of effluent (fluids, secretions, air) from a SURGICAL ANASTOMOSIS of the digestive, respiratory, g… | Pathologic Condition | Pathology | Base domain | AMW:DIS:230198 |
| Ancylostomiasis Infection of humans or animals with hookworms of the genus ANCYLOSTOMA. Characteristics include anemia, dyspepsia, eosinophilia, and abdominal swelli… | Infectious Disorder | Pathology | Base domain | AMW:DIS:010462 |
| Andersen Syndrome A form of inherited long QT syndrome (or LQT7) that is characterized by a triad of potassium-sensitive periodic paralysis, VENTRICULAR ECTOPIC BEATS,… | Syndrome | Pathology | Base domain | AMW:DIS:140072 |
| Androgen-Insensitivity Syndrome A disorder of sexual development transmitted as an X-linked recessive trait. These patients have a karyotype of 46,XY with end-organ resistance to an… | Syndrome | Pathology | Base domain | AMW:DIS:120070 |
| Anemia A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN. | Disorder | Pathology | Base domain | 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 | Base domain | 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 | Base domain | 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 | Base domain | 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 | Base domain | 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 | Base domain | AMW:DIS:150009 |
| Anemia, Hemolytic, Congenital Hemolytic anemia due to various intrinsic defects of the erythrocyte. | Congenital Disorder | Pathology | Base domain | 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 | Base domain | 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 | Base domain | 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 | Base domain | 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 | Base domain | 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 | Base domain | 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 | Base domain | 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 | Base domain | AMW:DIS:150032 |
| Anemia, Neonatal The mildest form of erythroblastosis fetalis in which anemia is the chief manifestation. | Congenital Disorder | Pathology | Base domain | 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 | Base domain | AMW:DIS:150031 |
| Anemia, Refractory A severe sometimes chronic anemia, usually macrocytic in type, that does not respond to ordinary antianemic therapy. | Disorder | Pathology | Base domain | 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 | Base domain | 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 | Base domain | AMW:DIS:150013 |
| Anemia, Sideroblastic Anemia characterized by the presence of erythroblasts containing excessive deposits of iron in the marrow. | Disorder | Pathology | Base domain | AMW:DIS:150038 |
| Anencephaly A malformation of the nervous system caused by failure of the anterior neuropore to close. Infants are born with intact spinal cords, cerebellums, an… | Congenital Disorder | Pathology | Base domain | AMW:DIS:100402 |
| Anetoderma Benign DERMATOSIS caused by a loss of dermal ELASTIC TISSUE resulting in localized sac-like areas of flaccid skin. It can be either primary (idiopath… | Disorder | Pathology | Base domain | AMW:DIS:170003 |
| Aneuploidy The chromosomal constitution of cells which deviate from the normal by the addition or subtraction of CHROMOSOMES, chromosome pairs, or chromosome fr… | Pathologic Condition | Pathology | Base domain | AMW:DIS:230051 |
| Aneurysm Pathological outpouching or sac-like dilatation in the wall of any blood vessel (ARTERIES or VEINS) or the heart (HEART ANEURYSM). It indicates a thi… | Vascular Disorder | Pathology | Base domain | AMW:DIS:140186 |
| Aneurysm, Aortic Arch An abnormal balloon- or sac-like dilatation in the wall of the AORTIC ARCH. | Vascular Disorder | Pathology | Base domain | AMW:DIS:140193 |
| Aneurysm, Ascending Aorta An abnormal balloon- or sac-like dilatation in the wall of the ASCENDING AORTA. | Vascular Disorder | Pathology | Base domain | AMW:DIS:140195 |