Public registry
Nodes
Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Secondary membership only
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| Corneal Perforation A puncture or hole through the CORNEAL STROMA resulting from various diseases or trauma. | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100656 |
| Corticobasal Degeneration The label is process-shaped, but the organ-specific concept may also function as a disorder; manual semantic review is required. | Pathological process | Pathology | Nervous System [curated_secondary] | AMW:PROC:135078 |
| Cranial Nerve Diseases Disorders of one or more of the twelve cranial nerves. With the exception of the optic and olfactory nerves, this includes disorders of the brain ste… | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100335 |
| Cranial Nerve Injuries Dysfunction of one or more cranial nerves causally related to a traumatic injury. Penetrating and nonpenetrating CRANIOCEREBRAL TRAUMA; NECK INJURIES… | Traumatic Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100340 |
| Craniocerebral Trauma Traumatic injuries involving the cranium and intracranial structures (i.e., BRAIN; CRANIAL NERVES; MENINGES; and other structures). Injuries may be c… | Traumatic Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100651 |
| Cri-du-Chat Syndrome An infantile syndrome characterized by a cat-like cry, failure to thrive, microcephaly, MENTAL RETARDATION, spastic quadriparesis, micro- and retrogn… | Syndrome | Pathology | Nervous System [curated_secondary] | AMW:DIS:100486 |
| Cubital Tunnel Syndrome Compression of the ULNAR NERVE in the cubital tunnel, which is formed by the two heads of the flexor carpi ulnaris muscle, humeral-ulnar aponeurosis,… | Syndrome | Pathology | Nervous System [curated_secondary] | AMW:DIS:100599 |
| Dandy-Walker Syndrome A congenital abnormality of the central nervous system marked by failure of the midline structures of the cerebellum to develop, dilation of the four… | Syndrome | Pathology | Nervous System [curated_secondary] | AMW:DIS:100158 |
| De Lange Syndrome A syndrome characterized by growth retardation, severe MENTAL RETARDATION, short stature, a low-pitched growling cry, brachycephaly, low-set ears, we… | Syndrome | Pathology | Nervous System [curated_secondary] | AMW:DIS:100487 |
| Decerebrate State A condition characterized by abnormal posturing of the limbs that is associated with injury to the brainstem. This may occur as a clinical manifestat… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100434 |
| Delirium A disorder characterized by CONFUSION; inattentiveness; disorientation; ILLUSIONS; HALLUCINATIONS; agitation; and in some instances autonomic nervous… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100476 |
| Dementia An acquired organic mental disorder with loss of intellectual abilities of sufficient severity to interfere with social or occupational functioning. … | Degenerative Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100226 |
| Dementia, Multi-Infarct Loss of higher cortical functions with retained awareness due to multiple cortical or subcortical CEREBRAL INFARCTION. Memory, judgment, attention sp… | Vascular Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100169 |
| Dementia, Vascular An imprecise term referring to dementia associated with CEREBROVASCULAR DISORDERS, including CEREBRAL INFARCTION (single or multiple), and conditions… | Vascular Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100189 |
| Demyelinating Autoimmune Diseases, CNS Conditions characterized by loss or dysfunction of myelin (see MYELIN SHEATH) in the brain, spinal cord, or optic nerves secondary to autoimmune medi… | Immune Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100004 |
| Demyelinating Diseases Diseases characterized by loss or dysfunction of myelin in the central or peripheral nervous system. | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100374 |
| Diabetic Neuropathies Peripheral, autonomic, and cranial nerve disorders that are associated with DIABETES MELLITUS. These conditions usually result from diabetic microvas… | Metabolic Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100585 |
| Diaschisis Loss or decreased brain function within intact region of the brain distant from the site of the lesion. | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100236 |
| 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 | Nervous System [curated_secondary] | 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 | Nervous System [curated_secondary] | AMW:DIS:100005 |
| 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 | Nervous System [curated_secondary] | AMW:PROC:135074 |
| Diplopia A visual symptom in which a single object is perceived by the visual cortex as two objects rather than one. Disorders associated with this condition … | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100570 |
| Disorders of Excessive Somnolence Disorders characterized by hypersomnolence during normal waking hours that may impair cognitive functioning. Subtypes include primary hypersomnia dis… | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100634 |
| Down Syndrome A chromosome disorder associated either with an extra CHROMOSOME 21 or an effective TRISOMY for chromosome 21. Clinical manifestations include HYPOTO… | Syndrome | Pathology | Nervous System [curated_secondary] | AMW:DIS:100488 |
| Drug Resistant Epilepsy Epileptic condition in which adequate trials of two tolerated and appropriately chosen and used ANTIEPILEPTIC DRUGS schedules to achieve sustained se… | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100240 |
| Drug-Induced Parkinsonism Drug-induced parkinsonism used as a ClinicalGraph target concept for pathology / differential. | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100675 |
| Duane Retraction Syndrome A syndrome characterized by marked limitation of abduction of the eye, variable limitation of adduction and retraction of the globe, and narrowing of… | Syndrome | Pathology | Nervous System [curated_secondary] | AMW:DIS:100355 |
| Dysarthria Disorders of speech articulation caused by imperfect coordination of pharynx, larynx, tongue, or face muscles. This may result from CRANIAL NERVE DIS… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100468 |
| Dysautonomia, Familial An autosomal disorder of the peripheral and autonomic nervous systems limited to individuals of Ashkenazic Jewish descent. Clinical manifestations ar… | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100034 |
| Dysgeusia A condition characterized by alterations of the sense of taste which may range from mild to severe, including gross distortions of taste quality. | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100564 |