Public registry
Nodes
Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Any direct membership
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| Intracranial Hypotension Reduction of CEREBROSPINAL FLUID pressure characterized clinically by ORTHOSTATIC HEADACHE and occasionally by an ABDUCENS NERVE PALSY; HEARING LOSS;… | Vascular Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100298 |
| Intracranial 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 | Neurology [curated_secondary] | AMW:PROC:125033 |
| Isaacs Syndrome A rare neuromuscular disorder with onset usually in late childhood or early adulthood, characterized by intermittent or continuous widespread involun… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:050250 |
| Ischemic Attack, Transient Brief reversible episodes of focal, nonconvulsive ischemic dysfunction of the brain having a duration of less than 24 hours, and usually less than on… | Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100174 |
| Ischemic Stroke Stroke due to BRAIN ISCHEMIA resulting in interruption or reduction of blood flow to a part of the brain. When obstruction is due to a BLOOD CLOT for… | Vascular Disorder | Pathology | Neurology [role_derived] | AMW:DIS:100220 |
| Jaw Fractures Fractures of the upper or lower jaw. | Traumatic Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100662 |
| Jet Lag Syndrome A chronobiologic disorder resulting from rapid travel across a number of time zones, characterized by insomnia or hypersomnolence, fatigue, behaviora… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100332 |
| Kearns-Sayre Syndrome A mitochondrial disorder featuring the triad of chronic progressive EXTERNAL OPHTHALMOPLEGIA, cardiomyopathy (CARDIOMYOPATHIES) with conduction block… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:050257 |
| Kernicterus A term used pathologically to describe BILIRUBIN staining of the BASAL GANGLIA; BRAIN STEM; and CEREBELLUM and clinically to describe a syndrome asso… | Congenital Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100130 |
| Kleine-Levin Syndrome A rare condition characterized by recurrent hypersomnias associated with hyperphagia, occurring primarily in males in the second to third decade of l… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100636 |
| Kluver-Bucy Syndrome A neurobehavioral syndrome associated with bilateral medial temporal lobe dysfunction. Clinical manifestations include oral exploratory behavior; tac… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100234 |
| Korsakoff Syndrome An acquired cognitive disorder characterized by inattentiveness and the inability to form short term memories. This disorder is frequently associated… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100504 |
| Lafora Disease A form of stimulus sensitive MYOCLONIC EPILEPSY inherited as an autosomal recessive condition. The most common presenting feature is a single seizure… | Congenital Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100252 |
| Landau-Kleffner Syndrome A syndrome characterized by the onset of isolated language dysfunction in otherwise normal children (age of onset 4-7 years) and epileptiform dischar… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100261 |
| Language Development Disorders Conditions characterized by language abilities (comprehension and expression of speech and writing) that are below the expected level for a given age… | Pathologic Condition | Pathology | Neurology [curated_secondary] | AMW:DIS:100460 |
| Language Disorders Conditions characterized by deficiencies of comprehension or expression of written and spoken forms of language. These include acquired and developme… | Pathologic Condition | Pathology | Neurology [curated_secondary] | AMW:DIS:100454 |
| Lateral Medullary Syndrome INFARCTION of the dorsolateral aspect of MEDULLA OBLONGATA in the BRAIN STEM. It is caused by occlusion of the VERTEBRAL ARTERY and/or the posterior … | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100166 |
| Lateral Sinus 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 | Neurology [curated_secondary] | AMW:PROC:125035 |
| Laurence-Moon Syndrome An autosomal recessive condition characterized by hypogonadism; spinocerebellar degeneration; MENTAL RETARDATION; RETINITIS PIGMENTOSA; and OBESITY. … | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100283 |
| Lead Poisoning, Nervous System Injury to the nervous system secondary to exposure to lead compounds. Two distinct clinical patterns occur in children (LEAD POISONING, NERVOUS SYSTE… | Toxic Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100624 |
| Lead Poisoning, Nervous System, Adult Neurologic conditions in adults associated with acute or chronic exposure to lead or any of its salts. The most common lead related neurologic syndro… | Toxic Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100625 |
| Lead Poisoning, Nervous System, Childhood Neurologic disorders occurring in children following lead exposure. The most frequent manifestation of childhood lead toxicity is an encephalopathy a… | Toxic Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100626 |
| Leigh Disease A group of metabolic disorders primarily of infancy characterized by the subacute onset of psychomotor retardation, hypotonia, ataxia, weakness, visi… | Congenital Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100090 |
| Lennox Gastaut Syndrome A childhood-onset epilepsy syndrome. | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100262 |
| Lesch-Nyhan Syndrome An inherited disorder transmitted as a sex-linked trait and caused by a deficiency of an enzyme of purine metabolism; HYPOXANTHINE PHOSPHORIBOSYLTRAN… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100091 |
| Lethargy A general state of sluggishness, listless, or uninterested, with being tired, and having difficulty concentrating and doing simple tasks. It may be r… | Pathologic Condition | Pathology | Neurology [curated_secondary] | AMW:DIS:100498 |
| Leukoaraiosis Non-specific white matter changes in the BRAIN, often seen after age 65. Changes include loss of AXONS; MYELIN pallor, GLIOSIS, loss of ependymal cel… | Pathologic Condition | Pathology | Neurology [curated_secondary] | AMW:DIS:230173 |
| Leukodystrophy, Globoid Cell An autosomal recessive metabolic disorder caused by a deficiency of GALACTOSYLCERAMIDASE leading to intralysosomal accumulation of galactolipids such… | Congenital Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100084 |
| Leukodystrophy, Metachromatic An autosomal recessive metabolic disease caused by a deficiency of CEREBROSIDE-SULFATASE leading to intralysosomal accumulation of cerebroside sulfat… | Congenital Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100085 |
| Leukoencephalitis, Acute Hemorrhagic A fulminant and often fatal demyelinating disease of the brain which primarily affects young adults and children. Clinical features include the rapid… | Inflammatory Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100007 |