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Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Domain and all descendants
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| AIDS-Associated Nephropathy Renal syndrome in human immunodeficiency virus-infected patients characterized by nephrotic syndrome, severe proteinuria, focal and segmental glomeru… | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010362 |
| AIDS-Related Complex A prodromal phase of infection with the human immunodeficiency virus (HIV). Laboratory criteria separating AIDS-related complex (ARC) from AIDS inclu… | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010363 |
| AIDS-Related Opportunistic Infections Opportunistic infections found in patients who test positive for human immunodeficiency virus (HIV). The most common include PNEUMOCYSTIS PNEUMONIA, … | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010364 |
| Airway Obstruction Any hindrance to the passage of air into and out of the lungs. | Disorder | Pathology | Respiratory Medicine [curated_secondary] | AMW:DIS:080136 |
| Airway Remodeling The label denotes a pathological biological process or mechanism, not a disease entity. | Pathological process | Pathology | Respiratory Medicine [curated_secondary] | AMW:PROC:155015 |
| Alagille Syndrome A multisystem disorder that is characterized by aplasia of intrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC), and malformations in the cardiovascula… | Syndrome | Pathology | Gastroenterology [curated_secondary] | AMW:DIS:060009 |
| Aleutian Mink Disease A slow progressive disease of mink caused by the ALEUTIAN MINK DISEASE VIRUS. It is characterized by poor reproduction, weight loss, autoimmunity, hy… | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010666 |
| Aliivibrio Infections Infections with bacteria of the genus ALIIVIBRIO. | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010039 |
| Alkalosis A pathological condition that removes acid or adds base to the body fluids. | Metabolic Disorder | Pathology | Nephrology [curated_secondary] | AMW:DIS:180008 |
| Alkalosis, Respiratory A state due to excess loss of carbon dioxide from the body. (Dorland, 27th ed) | Metabolic Disorder | Pathology | Respiratory Medicine [curated_secondary] | AMW:DIS:080131 |
| Allergic Fungal Sinusitis Fungal infection in the PARANASAL SINUSES characterized by common allergy respiratory symptoms, recurrent NASAL POLYPS and/or ASTHMA with buildup of … | Immune Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010234 |
| alpha 1-Antitrypsin Deficiency Deficiency of the protease inhibitor ALPHA 1-ANTITRYPSIN that manifests primarily as PULMONARY EMPHYSEMA and LIVER CIRRHOSIS. | Congenital Disorder | Pathology | Gastroenterology [curated_secondary] | AMW:DIS:060176 |
| 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 | Haematology [curated_secondary] | AMW:DIS:150023 |
| Alphavirus Infections Virus diseases caused by members of the ALPHAVIRUS genus of the family TOGAVIRIDAE. | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010616 |
| Alternariosis Opportunistic fungal infection by a member of ALTERNARIA genus. | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010257 |
| Altitude Sickness Multiple symptoms associated with reduced oxygen at high ALTITUDE. | Exposure Related Disorder | Pathology | Respiratory Medicine [curated_secondary] | AMW:DIS:080117 |
| Alveolitis, Extrinsic Allergic A common interstitial lung disease caused by hypersensitivity reactions of PULMONARY ALVEOLI after inhalation of and sensitization to environmental a… | Immune Disorder | Pathology | Respiratory Medicine [curated_secondary] | AMW:DIS:080047 |
| Amebiasis Infection with any of various amebae. It is an asymptomatic carrier state in most individuals, but diseases ranging from chronic, mild diarrhea to fu… | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010503 |
| Amyloidosis A group of sporadic, familial and/or inherited, degenerative, and infectious disease processes, linked by the common theme of abnormal protein foldin… | Metabolic Disorder | Pathology | Metabolic Medicine [curated_secondary] | AMW:DIS:180053 |
| Anaphylaxis An acute hypersensitivity reaction due to exposure to a previously encountered ANTIGEN. The reaction may include rapidly progressing URTICARIA, respi… | Immune Disorder | Pathology | Rheumatology [curated_secondary] | AMW:DIS:200014 |
| Anaplasmataceae Infections Infections with bacteria of the family ANAPLASMATACEAE. | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010040 |
| Anaplasmosis A disease usually in cattle caused by parasitization of the red blood cells by bacteria of the genus ANAPLASMA. | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010041 |
| Ancylostomiasis Infection of humans or animals with hookworms of the genus ANCYLOSTOMA. Characteristics include anemia, dyspepsia, eosinophilia, and abdominal swelli… | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | 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 | Cardiology [curated_secondary] | 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 | Endocrinology [curated_secondary] | AMW:DIS:120070 |
| Anemia A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN. | Disorder | Pathology | Haematology [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 | Haematology [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 | Haematology [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 | Haematology [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 | Haematology [curated_secondary] | AMW:DIS:150008 |