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715 results

Current membership scope: Domain and all descendants

ConceptNode typeBase domainMatched membershipIdentifier
Leukoencephalopathies
Any of various diseases affecting the white matter of the central nervous system.
DisorderPathologyNeurology [curated_secondary]AMW:DIS:100299
Leukomalacia, Periventricular
Degeneration of white matter adjacent to the CEREBRAL VENTRICLES following cerebral hypoxia or BRAIN ISCHEMIA in neonates. The condition primarily af…
Congenital DisorderPathologyNeurology [curated_secondary]AMW:DIS:100216
Lewy Body Disease
A neurodegenerative disease characterized by dementia, mild parkinsonism, and fluctuations in attention and alertness. The neuropsychiatric manifesta…
DisorderPathologyNeurology [curated_secondary]AMW:DIS:100063
Lissencephaly
A smooth brain malformation of the CEREBRAL CORTEX resulting from the abnormal location of developing neurons during corticogenesis. It is characteri…
Congenital DisorderPathologyNeurology [curated_secondary]AMW:DIS:100394
Locked-In Syndrome
Acquired neuromuscular disorder characterized by complete paralysis of voluntary muscles and lower CRANIAL NERVES except for limited voluntary eye mo…
SyndromePathologyNeurology [curated_secondary]AMW:DIS:100538
Lysosomal Storage Diseases, Nervous System
A group of enzymatic disorders affecting the nervous system and to a variable degree the skeletal system, lymphoreticular system, and other organs. T…
Congenital DisorderPathologyNeurology [curated_secondary]AMW:DIS:100092
Machado-Joseph Disease
A dominantly-inherited ATAXIA first described in people of Azorean and Portuguese descent, and subsequently identified in Brazil, Japan, China, and A…
Congenital DisorderPathologyNeurology [curated_secondary]AMW:DIS:100156
Malformations of Cortical Development
Abnormalities in the development of the CEREBRAL CORTEX. These include malformations arising from abnormal neuronal and glial CELL PROLIFERATION or A…
Congenital DisorderPathologyNeurology [curated_secondary]AMW:DIS:100388
Malformations of Cortical Development, Group I
Cortical malformations secondary to abnormal neuronal and glial CELL PROLIFERATION or APOPTOSIS in NEUROGENESIS. This group includes congenital MICRO…
Congenital DisorderPathologyNeurology [curated_secondary]AMW:DIS:100389
Malformations of Cortical Development, Group II
Cortical malformations secondary to abnormal neuronal CELL MIGRATION in NEUROGENESIS. This group includes COBBLESTONE LISSENCEPHALY and PERIVENTRICUL…
Congenital DisorderPathologyNeurology [curated_secondary]AMW:DIS:100392
Malformations of Cortical Development, Group III
Cortical malformations secondary to abnormal cortical maturation after CELL MIGRATION in NEUROGENESIS. This group includes injury to the cortex durin…
Congenital DisorderPathologyNeurology [curated_secondary]AMW:DIS:100398
Mandibular Fractures
Fractures of the lower jaw.
Traumatic DisorderPathologyNeurology [curated_secondary]AMW:DIS:100663
Mandibular Injuries
Injuries to the lower jaw bone.
Traumatic DisorderPathologyNeurology [curated_secondary]AMW:DIS:100665
Manganese Poisoning
Manganese poisoning is associated with chronic inhalation of manganese particles by individuals who work with manganese ore. Clinical features includ…
Toxic DisorderPathologyNeurology [curated_secondary]AMW:DIS:100627
Mania
A state of elevated excitement with over-activity sometimes accompanied with psychotic symptoms (e.g., PSYCHOMOTOR AGITATION, inflated SELF ESTEEM an…
Pathologic ConditionPathologyNeurology [curated_secondary]AMW:DIS:100499
Maple Syrup Urine Disease
An autosomal recessive inherited disorder with multiple forms of phenotypic expression, caused by a defect in the oxidative decarboxylation of branch…
Congenital DisorderPathologyNeurology [curated_secondary]AMW:DIS:100113
Marchiafava-Bignami Disease
A neurodegenerative condition that is characterized by demyelination or necrosis of the CORPUS CALLOSUM. Symptoms include DEPRESSION; PARANOIA; DEMEN…
DisorderPathologyNeurology [curated_secondary]AMW:DIS:100131
Maxillary Fractures
Fractures of the upper jaw.
Traumatic DisorderPathologyNeurology [curated_secondary]AMW:DIS:100664
Maxillofacial Injuries
General or unspecified injuries involving the face and jaw (either upper, lower, or both).
Traumatic DisorderPathologyNeurology [curated_secondary]AMW:DIS:100661
Median Neuropathy
Disease involving the median nerve, from its origin at the BRACHIAL PLEXUS to its termination in the hand. Clinical features include weakness of wris…
DisorderPathologyNeurology [curated_secondary]AMW:DIS:100589
Megalencephaly
A congenital abnormality in which the occipitofrontal circumference is greater than two standard deviations above the mean for a given age. It is ass…
Congenital DisorderPathologyNeurology [curated_secondary]AMW:DIS:050315
Meige Syndrome
A syndrome characterized by orofacial DYSTONIA; including BLEPHAROSPASM; forceful jaw opening; lip retraction; platysma muscle spasm; and tongue prot…
SyndromePathologyNeurology [curated_secondary]AMW:DIS:100059
MELAS Syndrome
A mitochondrial disorder characterized by focal or generalized seizures, episodes of transient or persistent neurologic dysfunction resembling stroke…
SyndromePathologyNeurology [curated_secondary]AMW:DIS:050254
Memory Disorders
Disturbances in registering an impression, in the retention of an acquired impression, or in the recall of an impression. Memory impairments are asso…
Pathologic ConditionPathologyNeurology [curated_secondary]AMW:DIS:100500
Meningism
A condition characterized by neck stiffness, headache, and other symptoms suggestive of meningeal irritation, but without actual inflammation of the …
Pathologic ConditionPathologyNeurology [curated_secondary]AMW:DIS:100449
Meningitis
Inflammation of the coverings of the brain and/or spinal cord, which consist of the PIA MATER; ARACHNOID; and DURA MATER. Infections (viral, bacteria…
Inflammatory DisorderPathologyNeurology [role_derived]AMW:DIS:100426
Meningitis, Aseptic
A syndrome characterized by headache, neck stiffness, low grade fever, and CSF lymphocytic pleocytosis in the absence of an acute bacterial pathogen.…
Inflammatory DisorderPathologyNeurology [curated_secondary]AMW:DIS:100428
Meningocele
A congenital or acquired protrusion of the meninges, unaccompanied by neural tissue, through a bony defect in the skull or vertebral column.
Congenital DisorderPathologyNeurology [curated_secondary]AMW:DIS:100405
Meningomyelocele
Congenital, or rarely acquired, herniation of meningeal and spinal cord tissue through a bony defect in the vertebral column. The majority of these d…
Congenital DisorderPathologyNeurology [curated_secondary]AMW:DIS:100406
Menkes Kinky Hair Syndrome
An inherited disorder of copper metabolism transmitted as an X-linked trait and characterized by the infantile onset of HYPOTHERMIA, feeding difficul…
SyndromePathologyNeurology [curated_secondary]AMW:DIS:100114