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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 |
|---|---|---|---|---|
| Communicable Diseases, Emerging Infectious diseases that are novel in their outbreak ranges (geographic and host) or transmission mode. | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010369 |
| Communicable Diseases, Imported Infectious diseases originating in one geographically delineated ecosystem that are carried (by travel or immigration) to another geographically deli… | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010370 |
| Community-Acquired Infections Any infection acquired in the community, that is, contrasted with those acquired in a health care facility (CROSS INFECTION). An infection would be c… | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010377 |
| Community-Acquired Pneumonia Infection of the lungs in a patient who is not hospitalized or who has not resided in a long-term care facility for 14 days prior to the onset of sym… | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010378 |
| Condylomata Acuminata Sexually transmitted form of anogenital warty growth caused by the HUMAN PAPILLOMAVIRUS VIRUSES. | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010375 |
| Congenital Bone Marrow Failure Syndromes Inherited syndromes characterized by deficiency or absence of various blood cells due to mutations that affect HEMATOPOIETIC STEM CELLS development a… | Syndrome | Pathology | Haematology [curated_secondary] | AMW:DIS:150098 |
| Congenital Hyperinsulinism A familial, nontransient HYPOGLYCEMIA with defects in negative feedback of GLUCOSE-regulated INSULIN release. Clinical phenotypes include HYPOGLYCEMI… | Congenital Disorder | Pathology | Gastroenterology [curated_secondary] | AMW:DIS:060219 |
| Congenital Hypothyroidism A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, s… | Metabolic Disorder | Pathology | Endocrinology [curated_secondary] | AMW:DIS:050010 |
| Congenital Portosystemic Shunt Congenital vascular malformation where the portal venous system blood (PORTAL SYSTEM) bypasses the liver sinusoids and drains into the systemic vein … | Congenital Disorder | Pathology | Cardiology [curated_secondary] | AMW:DIS:140042 |
| Congenitally Corrected Transposition of the Great Arteries A rare heart defect that occurs when the HEART VENTRICLES and attached valves, the MITRAL VALVE and the TRICUSPID VALVE are reversed so that the AORT… | Congenital Disorder | Pathology | Cardiology [curated_secondary] | AMW:DIS:140036 |
| Conjunctivitis, Acute Hemorrhagic A highly contagious disease characterized by subconjunctival hemorrhage, sudden swelling of the eyelids and congestion, redness, and pain in the eye.… | Inflammatory Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010387 |
| Conjunctivitis, Bacterial Purulent infections of the conjunctiva by several species of gram-negative, gram-positive, or acid-fast organisms. Some of the more commonly found ge… | Inflammatory Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010028 |
| Conjunctivitis, Inclusion An infection of the eyes characterized by the presence in conjunctival epithelial cells of inclusion bodies indistinguishable from those of trachoma.… | Inflammatory Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010029 |
| Conjunctivitis, Viral Inflammation, often mild, of the conjunctiva caused by a variety of viral agents. Conjunctival involvement may be part of a systemic infection. | Inflammatory Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010386 |
| Connective Tissue Diseases A heterogeneous group of disorders, some hereditary, others acquired, characterized by abnormal structure or function of one or more of the elements … | Disorder | Pathology | Rheumatology [curated_secondary] | AMW:DIS:170002 |
| Constipation Primarily a patient-reported sensation, complaint or symptom rather than a disease entity. | Symptom | Clinical Medicine | Gastroenterology [curated_secondary] | AMW:SYM:145023 |
| Coproporphyria, Hereditary An autosomal dominant porphyria that is due to a deficiency of COPROPORPHYRINOGEN OXIDASE in the LIVER, the sixth enzyme in the 8-enzyme biosynthetic… | Congenital Disorder | Pathology | Gastroenterology [curated_secondary] | AMW:DIS:060211 |
| Cor Triatriatum A malformation of the heart in which the embryonic common PULMONARY VEIN was not incorporated into the LEFT ATRIUM leaving behind a perforated fibrom… | Congenital Disorder | Pathology | Cardiology [curated_secondary] | AMW:DIS:140009 |
| Corneal Ulcer Loss of epithelial tissue from the surface of the cornea due to progressive erosion and necrosis of the tissue; usually caused by bacterial, fungal, … | Pathologic Condition | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010383 |
| Coronary Aneurysm Abnormal balloon- or sac-like dilatation in the wall of CORONARY VESSELS. Most coronary aneurysms are due to CORONARY ATHEROSCLEROSIS, and the rest a… | Vascular Disorder | Pathology | Cardiology [curated_secondary] | AMW:DIS:140156 |
| Coronary Artery Disease Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause. | Disorder | Pathology | Cardiology [curated_secondary] | AMW:DIS:140157 |
| Coronary Disease An imbalance between myocardial functional requirements and the capacity of the CORONARY VESSELS to supply sufficient blood flow. It is a form of MYO… | Disorder | Pathology | Cardiology [curated_secondary] | AMW:DIS:140155 |
| Coronary Occlusion Complete blockage of blood flow through one of the CORONARY ARTERIES, usually from CORONARY ATHEROSCLEROSIS. | Disorder | Pathology | Cardiology [curated_secondary] | AMW:DIS:140158 |
| Coronary Restenosis Recurrent narrowing or constriction of a coronary artery following surgical procedures performed to alleviate a prior obstruction. | Pathologic Condition | Pathology | Cardiology [curated_secondary] | AMW:DIS:140160 |
| Coronary Stenosis Narrowing or constriction of a coronary artery. | Pathologic Condition | Pathology | Cardiology [curated_secondary] | AMW:DIS:140159 |
| Coronary Thrombosis The label is process-shaped, but the organ-specific concept may also function as a disorder; manual semantic review is required. | Pathological process | Pathology | Cardiology [curated_secondary] | AMW:PROC:125039 |
| Coronary Vasospasm Spasm of the large- or medium-sized coronary arteries. | Disorder | Pathology | Cardiology [curated_secondary] | AMW:DIS:140162 |
| Coronary Vessel Anomalies Malformations of CORONARY VESSELS, either arteries or veins. Included are anomalous origins of coronary arteries; ARTERIOVENOUS FISTULA; CORONARY ANE… | Congenital Disorder | Pathology | Cardiology [curated_secondary] | AMW:DIS:140010 |
| Coronary-Subclavian Steal Syndrome A complication of INTERNAL MAMMARY-CORONARY ARTERY ANASTOMOSIS whereby an occlusion or stenosis of the proximal SUBCLAVIAN ARTERY causes a reversal o… | Syndrome | Pathology | Cardiology [curated_secondary] | AMW:DIS:140163 |
| Coronaviridae Infections Virus diseases caused by CORONAVIRIDAE. | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010737 |