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 |
|---|---|---|---|---|
| Diabetic Angiopathies VASCULAR DISEASES that are associated with DIABETES MELLITUS. | Metabolic Disorder | Pathology | Base domain | AMW:DIS:140236 |
| Diabetic Cardiomyopathies Diabetes complications in which VENTRICULAR REMODELING in the absence of CORONARY ATHEROSCLEROSIS and hypertension results in cardiac dysfunctions, t… | Metabolic Disorder | Pathology | Base domain | AMW:DIS:140109 |
| Diabetic Coma A state of unconsciousness as a complication of diabetes mellitus. It occurs in cases of extreme HYPERGLYCEMIA or extreme HYPOGLYCEMIA as a complicat… | Metabolic Disorder | Pathology | Base domain | AMW:DIS:190013 |
| Diabetic Foot Common foot problems in persons with DIABETES MELLITUS, caused by any combination of factors such as DIABETIC NEUROPATHIES; PERIPHERAL VASCULAR DISEA… | Metabolic Disorder | Pathology | Base domain | AMW:DIS:140237 |
| Diabetic Ketoacidosis A life-threatening complication of diabetes mellitus, primarily of TYPE 1 DIABETES MELLITUS with severe INSULIN deficiency and extreme HYPERGLYCEMIA.… | Metabolic Disorder | Pathology | Base domain | AMW:DIS:180007 |
| Diabetic Nephropathies KIDNEY injuries associated with diabetes mellitus and affecting KIDNEY GLOMERULUS; ARTERIOLES; KIDNEY TUBULES; and the interstitium. Clinical signs i… | Metabolic Disorder | Pathology | Base domain | AMW:DIS:120097 |
| Diabetic Neuropathies Peripheral, autonomic, and cranial nerve disorders that are associated with DIABETES MELLITUS. These conditions usually result from diabetic microvas… | Metabolic Disorder | Pathology | Base domain | AMW:DIS:100585 |
| Diabetic Retinopathy Disease of the RETINA as a complication of DIABETES MELLITUS. It is characterized by the progressive microvascular complications, such as ANEURYSM, i… | Metabolic Disorder | Pathology | Base domain | AMW:DIS:110112 |
| Diaper Rash A type of irritant dermatitis localized to the area in contact with a diaper and occurring most often as a reaction to prolonged contact with urine, … | Disorder | Pathology | Base domain | AMW:DIS:170046 |
| Diaphragmatic Eventration A congenital abnormality characterized by the elevation of the DIAPHRAGM dome. It is the result of a thinned diaphragmatic muscle and injured PHRENIC… | Congenital Disorder | Pathology | Base domain | AMW:DIS:060033 |
| Diarrhea, Infantile DIARRHEA occurring in infants from newborn to 24-months old. | Pathologic Condition | Pathology | Base domain | AMW:DIS:230298 |
| Diaschisis Loss or decreased brain function within intact region of the brain distant from the site of the lesion. | Disorder | Pathology | Base domain | AMW:DIS:100236 |
| Diastasis, Bone Abnormal separation of bones, often from a LIGAMENT. | Traumatic Disorder | Pathology | Base domain | AMW:DIS:050224 |
| Diastasis, Muscle Abnormal separation of muscles. | Traumatic Disorder | Pathology | Base domain | AMW:DIS:050226 |
| Diastema An abnormal opening or fissure between two adjacent teeth. | Congenital Disorder | Pathology | Base domain | AMW:DIS:070104 |
| Dicrocoeliasis Infection with flukes of the genus Dicrocoelium. | Infectious Disorder | Pathology | Base domain | AMW:DIS:010471 |
| Dictyocaulus Infections Infection with nematodes of the genus DICTYOCAULUS. In deer, cattle, sheep, and horses the bronchi are the site of infestation. | Infectious Disorder | Pathology | Base domain | AMW:DIS:010426 |
| Dientamoebiasis Gastrointestinal infection with organisms of the genus DIENTAMOEBA. | Infectious Disorder | Pathology | Base domain | AMW:DIS:010484 |
| Diffuse Alveolar Damage 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:150014 |
| Diffuse Axonal Injury A relatively common sequela of blunt head injury, characterized by a global disruption of axons throughout the brain. Associated clinical features ma… | Traumatic Disorder | Pathology | Base domain | AMW:DIS:100140 |
| Diffuse Cerebral Sclerosis of Schilder A rare central nervous system demyelinating condition affecting children and young adults. Pathologic findings include a large, sharply defined, asym… | Degenerative Disorder | Pathology | Base domain | AMW:DIS:100005 |
| Diffuse Intrinsic Pontine Glioma A rare, aggressive brain tumor that forms in the GLIAL CELLS in the PONS. | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040258 |
| Diffuse Neurofibrillary Tangles with Calcification The label is process-shaped, but the organ-specific concept may also function as a disorder; manual semantic review is required. | Pathological process | Pathology | Base domain | AMW:PROC:135074 |
| DiGeorge Syndrome Congenital syndrome characterized by a wide spectrum of characteristics including the absence of the THYMUS and PARATHYROID GLANDS resulting in T-cel… | Syndrome | Pathology | Base domain | AMW:DIS:050309 |
| Digestive System Abnormalities Congenital structural abnormalities of the DIGESTIVE SYSTEM. | Congenital Disorder | Pathology | Base domain | AMW:DIS:060029 |
| Digestive System Diseases Diseases in any part of the GASTROINTESTINAL TRACT or the accessory organs (LIVER; BILIARY TRACT; PANCREAS). | Disorder | Pathology | Base domain | AMW:DIS:060001 |
| Digestive System Fistula An abnormal passage communicating between any components of the digestive system, or between any part of the digestive system and surrounding organ(s… | Pathologic Condition | Pathology | Base domain | AMW:DIS:060040 |
| Digestive System Neoplasms Tumors or cancer of the DIGESTIVE SYSTEM. | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040499 |
| Digital Dermatitis Highly contagious infectious dermatitis with lesions near the interdigital spaces usually in cattle. It causes discomfort and often severe lameness (… | Inflammatory Disorder | Pathology | Base domain | AMW:DIS:010228 |
| Dihydropyrimidine Dehydrogenase Deficiency An autosomal recessive disorder affecting DIHYDROPYRIMIDINE DEHYDROGENASE and causing familial pyrimidinemia. It is characterized by thymine-uracilur… | Congenital Disorder | Pathology | Base domain | AMW:DIS:160135 |