Public registry
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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 |
|---|---|---|---|---|
| Cerebral Amyloid Angiopathy, Familial A familial disorder marked by AMYLOID deposits in the walls of small and medium sized blood vessels of CEREBRAL CORTEX and MENINGES. | Congenital Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100078 |
| Cerebral Arterial Diseases Pathological conditions of intracranial ARTERIES supplying the CEREBRUM. These diseases often are due to abnormalities or pathological processes in t… | Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100191 |
| Cerebral Cortical Thinning Decrease in CEREBRAL CORTICAL THICKNESS. | Pathologic Condition | Pathology | Neurology [curated_secondary] | AMW:DIS:100433 |
| Cerebral Hemorrhage Bleeding into one or both CEREBRAL HEMISPHERES including the BASAL GANGLIA and the CEREBRAL CORTEX. It is often associated with HYPERTENSION and CRAN… | Vascular Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100204 |
| Cerebral Hemorrhage, Traumatic Bleeding into one or both CEREBRAL HEMISPHERES due to TRAUMA. Hemorrhage may involve any part of the CEREBRAL CORTEX and the BASAL GANGLIA. Depending… | Traumatic Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100138 |
| Cerebral Infarction The formation of an area of NECROSIS in the CEREBRUM caused by an insufficiency of arterial or venous blood flow. Infarcts of the cerebrum are genera… | Vascular Disorder | Pathology | Neurology [role_derived] | AMW:DIS:100167 |
| Cerebral Intraventricular Hemorrhage Bleeding within the CEREBRAL VENTRICLES. It is associated with intraventricular trauma, aneurysm, vascular malformations, hypertension and in VERY LO… | Vascular Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100205 |
| Cerebral Palsy A heterogeneous group of nonprogressive motor disorders caused by chronic brain injuries that originate in the prenatal period, perinatal period, or … | Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100072 |
| Cerebral Small Vessel Diseases Pathological processes or diseases where cerebral MICROVESSELS show abnormalities. They are often associated with aging, hypertension and risk factor… | Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100184 |
| Cerebrospinal Fluid Leak Discharge of cerebrospinal fluid through a hole through the skull bone most commonly draining from the nose (CEREBROSPINAL FLUID RHINORRHEA) or the e… | Pathologic Condition | Pathology | Neurology [curated_secondary] | AMW:DIS:100430 |
| Cerebrospinal Fluid Otorrhea Discharge of cerebrospinal fluid through the external auditory meatus or through the eustachian tube into the nasopharynx. This is usually associated… | Pathologic Condition | Pathology | Neurology [curated_secondary] | AMW:DIS:100431 |
| Cerebrovascular Disorders A spectrum of pathological conditions of impaired blood flow in the brain. They can involve vessels (ARTERIES or VEINS) in the CEREBRUM, the CEREBELL… | Vascular Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100162 |
| Cerebrovascular Trauma Penetrating and nonpenetrating traumatic injuries to an extracranial or intracranial blood vessel that supplies the brain. This includes the CAROTID … | Traumatic Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100187 |
| Cervical Rib Syndrome A condition associated with compression of the BRACHIAL PLEXUS; SUBCLAVIAN ARTERY; and SUBCLAVIAN VEIN at the thoracic outlet and caused by a complet… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100605 |
| Charcot-Marie-Tooth Disease A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and l… | Congenital Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100384 |
| Charles Bonnet Syndrome Repetitive visual hallucinations experienced mostly by elderly with diminished visual acuity or visual field loss, with awareness of the fictional na… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100512 |
| Chorea Involuntary, forcible, rapid, jerky movements that may be subtle or become confluent, markedly altering normal patterns of movement. Hypotonia and pe… | Pathologic Condition | Pathology | Neurology [curated_secondary] | AMW:DIS:100309 |
| Chorea Gravidarum A rare movement disorder developed during PREGNANCY, characterized by involuntary jerky motion (CHOREA) and inability to maintain stable position of … | Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100056 |
| Chronic Traumatic Encephalopathy Degenerative brain disease linked to repetitive brain trauma. Progressive symptoms may include MEMORY LOSS; AGGRESSION; or DEPRESSION. | Traumatic Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100144 |
| Chronobiology Disorders Disruptions of the rhythmic cycle of bodily functions or activities. | Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100331 |
| Citrullinemia A group of diseases related to a deficiency of the enzyme ARGININOSUCCINATE SYNTHASE which causes an elevation of serum levels of CITRULLINE. In neon… | Congenital Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100127 |
| Classical Lissencephalies and Subcortical Band Heterotopias Disorders comprising a spectrum of brain malformations representing the paradigm of a diffuse neuronal migration disorder. They result in cognitive i… | Congenital Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100393 |
| Cobblestone Lissencephaly The smooth pebbled appearance of the CEREBRAL CORTEX with a thickened cortex and reduced and abnormal white matter, which results from migration of h… | Congenital Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100395 |
| Cockayne Syndrome A syndrome characterized by multiple system abnormalities including DWARFISM; PHOTOSENSITIVITY DISORDERS; PREMATURE AGING; and HEARING LOSS. It is ca… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:050009 |
| Coffin-Lowry Syndrome A rare, X-linked INTELLECTUAL DISABILITY syndrome that results from mutations in the RIBOSOMAL PROTEIN S6 KINASE gene. Typical manifestations of the … | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100490 |
| Cogan Syndrome A condition consisting of inflammatory eye disease usually presenting as interstitial KERATITIS, vestibuloauditory dysfunction, and large- to medium-… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100003 |
| Color Vision Defects Defects of color vision are mainly hereditary traits but can be secondary to acquired or developmental abnormalities in the CONES (RETINA). Severity … | Pathologic Condition | Pathology | Neurology [curated_secondary] | AMW:DIS:100569 |
| Coma A profound state of unconsciousness associated with depressed cerebral activity from which the individual cannot be aroused. Coma generally occurs wh… | Pathologic Condition | Pathology | Neurology [curated_secondary] | AMW:DIS:100480 |
| Coma, Post-Head Injury Prolonged unconsciousness from which the individual cannot be aroused, associated with traumatic injuries to the BRAIN. This may be defined as uncons… | Traumatic Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100481 |
| Complex Regional Pain Syndromes Conditions characterized by pain involving an extremity or other body region, HYPERESTHESIA, and localized autonomic dysfunction following injury to … | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100029 |