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 |
|---|---|---|---|---|
| Afibrinogenemia A deficiency or absence of FIBRINOGEN in the blood. | Congenital Disorder | Pathology | Base domain | AMW:DIS:150043 |
| Aflatoxin Poisoning Poisoning by AFLATOXINS most often associated with NAUSEA, abdominal pain, hepatotoxicity, immunosuppression, HEPATOCELLULAR CARCINOMA and sometimes … | Toxic Disorder | Pathology | Base domain | AMW:DIS:250031 |
| African Horse Sickness An insect-borne reovirus infection of horses, mules and donkeys in Africa and the Middle East; characterized by pulmonary edema, cardiac involvement,… | Infectious Disorder | Pathology | Base domain | AMW:DIS:010615 |
| African Swine Fever A sometimes fatal ASFIVIRUS infection of pigs, characterized by fever, cough, diarrhea, hemorrhagic lymph nodes, and edema of the gallbladder. It is … | Infectious Disorder | Pathology | Base domain | AMW:DIS:010629 |
| Agammaglobulinemia An immunologic deficiency state characterized by an extremely low level of generally all classes of gamma-globulin in the blood. | Immune Disorder | Pathology | Base domain | AMW:DIS:150084 |
| Agenesis of Corpus Callosum Birth defect that results in a partial or complete absence of the CORPUS CALLOSUM. It may be isolated or a part of a syndrome (e.g., AICARDI'S SYNDRO… | Congenital Disorder | Pathology | Base domain | AMW:DIS:100376 |
| Ageusia Complete or severe loss of the subjective sense of taste, frequently accompanied by OLFACTION DISORDERS. | Pathologic Condition | Pathology | Base domain | AMW:DIS:100563 |
| Aggressive Periodontitis Inflammation and loss of PERIODONTIUM that is characterized by rapid attachment loss and bone destruction in the presence of little local factors suc… | Inflammatory Disorder | Pathology | Base domain | AMW:DIS:070058 |
| Aging, Premature Changes in the organism associated with senescence, occurring at an accelerated rate. | Pathologic Condition | Pathology | Base domain | AMW:DIS:230220 |
| Agnosia Loss of the ability to comprehend the meaning or recognize the importance of various forms of stimulation that cannot be attributed to impairment of … | Pathologic Condition | Pathology | Base domain | AMW:DIS:100507 |
| Agranulocytosis A decrease in the number of GRANULOCYTES; (BASOPHILS; EOSINOPHILS; and NEUTROPHILS). | Disorder | Pathology | Base domain | AMW:DIS:150109 |
| Agraphia Loss or impairment of the ability to write (letters, syllables, words, or phrases) due to an injury to a specific cerebral area or occasionally due t… | Pathologic Condition | Pathology | Base domain | AMW:DIS:100455 |
| Agricultural Workers' Diseases Diseases in persons engaged in cultivating and tilling soil, growing plants, harvesting crops, raising livestock, or otherwise engaged in husbandry a… | Exposure Related Disorder | Pathology | Base domain | AMW:DIS:240002 |
| Aicardi Syndrome A rare genetic disorder characterized by partial or complete absence of the CORPUS CALLOSUM, resulting in infantile spasms, MENTAL RETARDATION, and l… | Syndrome | Pathology | Base domain | AMW:DIS:100378 |
| AIDS Arteritis, Central Nervous System Inflammation of ARTERIES in the CENTRAL NERVOUS SYSTEM that occurs in patients with ACQUIRED IMMUNODEFICIENCY SYNDROME or AIDS-RELATED OPPORTUNISTIC … | Inflammatory Disorder | Pathology | Base domain | AMW:DIS:010360 |
| AIDS Dementia Complex A neurologic condition associated with the ACQUIRED IMMUNODEFICIENCY SYNDROME and characterized by impaired concentration and memory, slowness of han… | Degenerative Disorder | Pathology | Base domain | AMW:DIS:010361 |
| AIDS-Associated Nephropathy Renal syndrome in human immunodeficiency virus-infected patients characterized by nephrotic syndrome, severe proteinuria, focal and segmental glomeru… | Infectious Disorder | Pathology | Base domain | 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 | Base domain | 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 | Base domain | AMW:DIS:010364 |
| Ainhum Spontaneous autoamputation of the fourth or fifth toe. | Disorder | Pathology | Base domain | AMW:DIS:050087 |
| Air In Pleural Cavity Created as a target node for a staged ClinicalGraph edge. Review and enrich this node later if needed. | Pathological finding | Pathology | Base domain | AMW:FIND:150003 |
| Airway Obstruction Any hindrance to the passage of air into and out of the lungs. | Disorder | Pathology | Base domain | AMW:DIS:080136 |
| Airway Remodeling The label denotes a pathological biological process or mechanism, not a disease entity. | Pathological process | Pathology | Base domain | AMW:PROC:155015 |
| airway smooth muscle hypertrophy Created as a target node for a staged ClinicalGraph edge. Review and enrich this node later if needed. | Morphological change | Pathology | Base domain | AMW:FIND:150004 |
| Akathisia, Drug-Induced A condition associated with the use of certain medications and characterized by an internal sense of motor restlessness often described as an inabili… | Toxic Disorder | Pathology | Base domain | AMW:DIS:100306 |
| Akinetic Mutism A syndrome characterized by a silent and inert state without voluntary motor activity despite preserved sensorimotor pathways and vigilance. Bilatera… | Disorder | Pathology | Base domain | AMW:DIS:100049 |
| Alagille Syndrome A multisystem disorder that is characterized by aplasia of intrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC), and malformations in the cardiovascula… | Syndrome | Pathology | Base domain | AMW:DIS:060009 |
| Albinism General term for a number of inherited defects of amino acid metabolism in which there is a deficiency or absence of pigment in the eyes, skin, or ha… | Congenital Disorder | Pathology | Base domain | AMW:DIS:110041 |
| Albinism, Ocular Albinism affecting the eye in which pigment of the hair and skin is normal or only slightly diluted. The classic type is X-linked (Nettleship-Falls),… | Congenital Disorder | Pathology | Base domain | AMW:DIS:110042 |
| Albinism, Oculocutaneous Heterogeneous group of autosomal recessive disorders comprising at least four recognized types, all having in common varying degrees of hypopigmentat… | Congenital Disorder | Pathology | Base domain | AMW:DIS:110043 |