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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 |
|---|---|---|---|---|
| Eye Infections, Parasitic Mild to severe infections of the eye and its adjacent structures (adnexa) by adult or larval protozoan or metazoan parasites. | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010410 |
| Eye Infections, Viral Infections of the eye caused by minute intracellular agents. These infections may lead to severe inflammation in various parts of the eye - conjuncti… | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010385 |
| Factor V Deficiency A deficiency of blood coagulation factor V (known as proaccelerin or accelerator globulin or labile factor) leading to a rare hemorrhagic tendency kn… | Congenital Disorder | Pathology | Haematology [curated_secondary] | AMW:DIS:150046 |
| Factor VII Deficiency An autosomal recessive characteristic or a coagulation disorder acquired in association with VITAMIN K DEFICIENCY. FACTOR VII is a Vitamin K dependen… | Congenital Disorder | Pathology | Haematology [curated_secondary] | AMW:DIS:150047 |
| Factor X Deficiency Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in… | Congenital Disorder | Pathology | Haematology [curated_secondary] | AMW:DIS:150048 |
| Factor XI Deficiency A hereditary deficiency of blood coagulation factor XI (also known as plasma thromboplastin antecedent or PTA or antihemophilic factor C) resulting i… | Congenital Disorder | Pathology | Haematology [curated_secondary] | AMW:DIS:150049 |
| Factor XII Deficiency An absence or reduced level of blood coagulation factor XII. It normally occurs in the absence of patient or family history of hemorrhagic disorders … | Congenital Disorder | Pathology | Haematology [curated_secondary] | AMW:DIS:150050 |
| Factor XIII Deficiency A deficiency of blood coagulation FACTOR XIII or fibrin stabilizing factor (FSF) that prevents blood clot formation and results in a clinical hemorrh… | Congenital Disorder | Pathology | Haematology [curated_secondary] | AMW:DIS:150051 |
| Failure to Thrive A condition of substandard growth or diminished capacity to maintain normal function. | Pathologic Condition | Pathology | Clinical Nutrition [curated_secondary] | AMW:DIS:230244 |
| Familial Hypophosphatemic Rickets A hereditary disorder characterized by HYPOPHOSPHATEMIA; RICKETS; OSTEOMALACIA; renal defects in phosphate reabsorption and vitamin D metabolism; and… | Congenital Disorder | Pathology | Endocrinology [curated_secondary], Nephrology [curated_secondary] | AMW:DIS:050080 |
| Familial Primary Pulmonary Hypertension Familial or idiopathic hypertension in the PULMONARY CIRCULATION which is not secondary to other disease. | Vascular Disorder | Pathology | Respiratory Medicine [curated_secondary] | AMW:DIS:080043 |
| Fanconi Anemia Congenital disorder affecting all bone marrow elements, resulting in ANEMIA; LEUKOPENIA; and THROMBOPENIA, and associated with cardiac, renal, and li… | Congenital Disorder | Pathology | Haematology [curated_secondary] | AMW:DIS:150007 |
| Fanconi Syndrome A hereditary or acquired form of generalized dysfunction of the PROXIMAL KIDNEY TUBULE without primary involvement of the KIDNEY GLOMERULUS. It is us… | Syndrome | Pathology | Nephrology [curated_secondary] | AMW:DIS:120147 |
| Farmer's Lung A form of alveolitis or pneumonitis due to an acquired hypersensitivity to inhaled antigens associated with farm environment. Antigens in the farm du… | Immune Disorder | Pathology | Respiratory Medicine [curated_secondary] | AMW:DIS:080049 |
| Fascioliasis Liver disease caused by infections with parasitic flukes of the genus FASCIOLA, such as FASCIOLA HEPATICA. | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010473 |
| Fascioloidiasis Infection of cattle and other herbivores with the giant liver fluke Fascioloides magna. It is characterized by extensive destruction of the liver par… | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010428 |
| Fatty Liver Lipid infiltration of the hepatic parenchymal cells resulting in a yellow-colored liver. The abnormal lipid accumulation is usually in the form of TR… | Disorder | Pathology | Gastroenterology [curated_secondary] | AMW:DIS:060180 |
| Fatty Liver, Alcoholic Lipid infiltration of the hepatic parenchymal cells that is due to ALCOHOL ABUSE. The fatty changes in the alcoholic fatty liver may be reversible, d… | Toxic Disorder | Pathology | Gastroenterology [curated_secondary] | AMW:DIS:060181 |
| Favism Hemolytic anemia due to the ingestion of fava beans or after inhalation of pollen from the Vicia fava plant by persons with glucose-6-phosphate dehyd… | Congenital Disorder | Pathology | Haematology [curated_secondary] | AMW:DIS:150019 |
| Febrile Neutropenia Fever accompanied by a significant reduction in the number of NEUTROPHILS. | Disorder | Pathology | Haematology [curated_secondary] | AMW:DIS:150111 |
| Fecal Impaction Formation of a firm impassable mass of stool in the RECTUM or distal COLON. | Disorder | Pathology | Gastroenterology [curated_secondary] | AMW:DIS:060131 |
| Fecal Incontinence Failure of voluntary control of the anal sphincters, with involuntary passage of feces and flatus. | Disorder | Pathology | Gastroenterology [curated_secondary] | AMW:DIS:060157 |
| Feline Acquired Immunodeficiency Syndrome Acquired defect of cellular immunity that occurs in cats infected with feline immunodeficiency virus (FIV) and in some cats infected with feline leuk… | Syndrome | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010766 |
| Feline Infectious Peritonitis Common coronavirus infection of cats caused by the feline infectious peritonitis virus (CORONAVIRUS, FELINE). The disease is characterized by a long … | Inflammatory Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010740 |
| Feline Panleukopenia A highly contagious DNA virus infection of the cat family, characterized by fever, enteritis and bone marrow changes. It is also called feline ataxia… | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010668 |
| Felty Syndrome A rare complication of rheumatoid arthritis with autoimmune NEUTROPENIA; and SPLENOMEGALY. | Syndrome | Pathology | Rheumatology [curated_secondary] | AMW:DIS:050195 |
| 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 | Haematology [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 | Haematology [curated_secondary] | AMW:DIS:150035 |
| Fibromuscular Dysplasia An idiopathic, segmental, nonatheromatous disease of the musculature of arterial walls, leading to STENOSIS of small and medium-sized arteries. There… | Pathologic Condition | Pathology | Cardiology [curated_secondary] | AMW:DIS:140230 |
| Fibromyalgia A common nonarticular rheumatic syndrome characterized by myalgia and multiple points of focal muscle tenderness to palpation (trigger points). Muscl… | Disorder | Pathology | Rheumatology [curated_secondary] | AMW:DIS:050249 |