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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 |
|---|---|---|---|---|
| Brain Stem Hemorrhage, Traumatic Bleeding into structures of BRAIN STEM, including the MIDBRAIN; PONS; or MEDULLA OBLONGATA, as the result of CRANIOCEREBRAL TRAUMA. DIFFUSE AXONAL IN… | Traumatic Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100137 |
| Brain Stem Infarctions Infarctions that occur in the BRAIN STEM which is comprised of the MIDBRAIN; PONS; and MEDULLA OBLONGATA. There are several named syndromes character… | Vascular Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100165 |
| Brown-Sequard Syndrome A syndrome associated with injury to the lateral half of the spinal cord. The condition is characterized by the following clinical features (which ar… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100535 |
| Bulbar Palsy, Progressive A motor neuron disease marked by progressive weakness of the muscles innervated by cranial nerves of the lower brain stem. Clinical manifestations in… | Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100419 |
| Bulbo-Spinal Atrophy, X-Linked An X-linked recessive form of spinal muscular atrophy. It is due to a mutation of the gene encoding the ANDROGEN RECEPTOR. | Degenerative Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100320 |
| CADASIL A familial, cerebral arteriopathy mapped to chromosome 19q12, and characterized by the presence of granular deposits in small CEREBRAL ARTERIES produ… | Congenital Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100168 |
| Canavan Disease A rare neurodegenerative condition of infancy or childhood characterized by white matter vacuolization and demeylination that gives rise to a spongy … | Congenital Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100083 |
| Carbamoyl-Phosphate Synthase I Deficiency Disease A urea cycle disorder manifesting in infancy as lethargy, emesis, seizures, alterations of muscle tone, abnormal eye movements, and an elevation of s… | Congenital Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100126 |
| Carotid Artery Diseases Pathological conditions involving the CAROTID ARTERIES, including the common, internal, and external carotid arteries. ATHEROSCLEROSIS and TRAUMA are… | Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100177 |
| Carotid Artery Injuries Damages to the CAROTID ARTERIES caused either by blunt force or penetrating trauma, such as CRANIOCEREBRAL TRAUMA; THORACIC INJURIES; and NECK INJURI… | Traumatic Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100178 |
| Carotid Artery Thrombosis Blood clot formation in any part of the CAROTID ARTERIES. This may produce CAROTID STENOSIS or occlusion of the vessel, leading to TRANSIENT ISCHEMIC… | Vascular Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100180 |
| Carotid Artery, Internal, Dissection The splitting of the vessel wall in one or both (left and right) internal carotid arteries (CAROTID ARTERY, INTERNAL). Interstitial hemorrhage into t… | Traumatic Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100179 |
| Carotid Stenosis Narrowing or stricture of any part of the CAROTID ARTERIES, most often due to atherosclerotic plaque formation. Ulcerations may form in atherosclerot… | Pathologic Condition | Pathology | Neurology [curated_secondary] | AMW:DIS:100181 |
| Carotid Webs The presence of one or more thin flap-like membranes arising from the posterior wall of the INTERNAL CAROTID ARTERY bulb. While carotid webs can be a… | Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100182 |
| Carotid-Cavernous Sinus Fistula An acquired or spontaneous abnormality in which there is communication between CAVERNOUS SINUS, a venous structure, and the CAROTID ARTERIES. It is o… | Pathologic Condition | Pathology | Neurology [curated_secondary] | AMW:DIS:100149 |
| Carpal Tunnel Syndrome Entrapment of the MEDIAN NERVE in the carpal tunnel, which is formed by the flexor retinaculum and the CARPAL BONES. This syndrome may be associated … | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100590 |
| Catalepsy A condition characterized by inactivity, decreased responsiveness to stimuli, and a tendency to maintain an immobile posture. The limbs tend to remai… | Pathologic Condition | Pathology | Neurology [curated_secondary] | AMW:DIS:100438 |
| Cataplexy A condition characterized by transient weakness or paralysis of somatic musculature triggered by an emotional stimulus or physical exertion. Cataplex… | Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100638 |
| Catatonia A neuropsychiatric disorder characterized by one or more of the following essential features: immobility, mutism, negativism (active or passive refus… | Pathologic Condition | Pathology | Neurology [curated_secondary] | AMW:DIS:100452 |
| Cauda Equina Syndrome Compressive lesion affecting the nerve roots of the CAUDA EQUINA (e.g., compression, herniation, inflammation, rupture, or stenosis), which controls … | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100602 |
| Causalgia A complex regional pain syndrome characterized by burning pain and marked sensitivity to touch (HYPERESTHESIA) in the distribution of an injured peri… | Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100030 |
| Cavernous Sinus Syndromes Disease processes of the CAVERNOUS SINUS. | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100148 |
| Cavernous Sinus Thrombosis Formation or presence of a blood clot (THROMBUS) in the CAVERNOUS SINUS of the brain. Infections of the paranasal sinuses and adjacent structures, CR… | Vascular Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100150 |
| Central Cord Syndrome A syndrome associated with traumatic injury to the cervical or upper thoracic regions of the spinal cord characterized by weakness in the arms with r… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100325 |
| Central Nervous System Diseases Diseases of any component of the brain (including the cerebral hemispheres, diencephalon, brain stem, and cerebellum) or the spinal cord. | Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100046 |
| Central Nervous System Vascular Malformations Congenital, inherited, or acquired abnormalities involving ARTERIES; VEINS; or venous sinuses in the BRAIN; SPINAL CORD; and MENINGES. | Vascular Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100379 |
| Cerebellar Ataxia Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movem… | Pathologic Condition | Pathology | Neurology [curated_secondary] | AMW:DIS:100153 |
| Cerebellar Cognitive Affective Syndrome Disease that affects linguistic, VISUAL SPATIAL PROCESSING; EXECUTIVE FUNCTION, and MOOD regulation. Cerebellar Cognitive Affective Syndrome is assoc… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100157 |
| Cerebellar Diseases Diseases that affect the structure or function of the cerebellum. Cardinal manifestations of cerebellar dysfunction include dysmetria, GAIT ATAXIA, a… | Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100152 |
| Cerebral Amyloid Angiopathy A heterogeneous group of sporadic or familial disorders characterized by AMYLOID deposits in the walls of small and medium sized blood vessels of CER… | Metabolic Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100192 |