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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 |
|---|---|---|---|---|
| Gerstmann Syndrome A disorder of cognition characterized by the tetrad of finger agnosia, dysgraphia, DYSCALCULIA, and right-left disorientation. The syndrome may be de… | Syndrome | Pathology | Nervous System [curated_secondary] | AMW:DIS:100508 |
| Giant Axonal Neuropathy Rare autosomal recessive disorder of INTERMEDIATE FILAMENT PROTEINS. The disease is caused by mutations in the gene that codes gigaxonin protein. The… | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100385 |
| Giant Cell Arteritis A systemic autoimmune disorder that typically affects medium and large ARTERIES, usually leading to occlusive granulomatous vasculitis with transmura… | Inflammatory Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100025 |
| Glossopharyngeal Nerve Diseases Diseases of the ninth cranial (glossopharyngeal) nerve or its nuclei in the medulla. The nerve may be injured by diseases affecting the lower brain s… | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100349 |
| Glossopharyngeal Nerve Injuries Traumatic injuries to the GLOSSOPHARYNGEAL NERVE. | Traumatic Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100341 |
| Glycogen Storage Disease Type II An autosomal recessively inherited glycogen storage disease caused by GLUCAN 1,4-ALPHA-GLUCOSIDASE deficiency. Large amounts of GLYCOGEN accumulate i… | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100094 |
| Glycogen Storage Disease Type IIb An X-linked dominant multisystem disorder resulting in cardiomyopathy, myopathy and INTELLECTUAL DISABILITY. It is caused by mutation in the gene enc… | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100492 |
| Guillain-Barre Syndrome An acute inflammatory autoimmune neuritis caused by T cell- mediated cellular immune response directed towards peripheral myelin. Demyelination occur… | Immune Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100019 |
| Hallucinations Subjectively experienced sensations in the absence of an appropriate stimulus, but which are regarded by the individual as real. They may be of organ… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100511 |
| Hand-Arm Vibration Syndrome An occupational disorder resulting from prolonged exposure to vibration, affecting the fingers, hands, and forearms. It occurs in workers who regular… | Syndrome | Pathology | Nervous System [curated_secondary] | AMW:DIS:100586 |
| Hartnup Disease An autosomal recessive disorder due to defective absorption of NEUTRAL AMINO ACIDS by both the intestine and the PROXIMAL RENAL TUBULES. The abnormal… | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100080 |
| Head Injuries, Closed Traumatic injuries to the cranium where the integrity of the skull is not compromised and no bone fragments or other objects penetrate the skull and … | Traumatic Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100668 |
| Head Injuries, Penetrating Head injuries which feature compromise of the skull and dura mater. These may result from gunshot wounds (WOUNDS, GUNSHOT), stab wounds (WOUNDS, STAB… | Traumatic Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100671 |
| Heavy Metal Poisoning, Nervous System Conditions associated with damage or dysfunction of the nervous system caused by exposure to heavy metals, which may cause a variety of central, peri… | Toxic Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100622 |
| Hematoma, Epidural, Cranial Accumulation of blood in the EPIDURAL SPACE between the SKULL and the DURA MATER, often as a result of bleeding from the MENINGEAL ARTERIES associate… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100208 |
| Hematoma, Epidural, Spinal A rare epidural hematoma in the spinal epidural space, usually due to a vascular malformation (CENTRAL NERVOUS SYSTEM VASCULAR MALFORMATIONS) or TRAU… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:230146 |
| Hematoma, Subdural Accumulation of blood in the SUBDURAL SPACE between the DURA MATER and the arachnoidal layer of the MENINGES. This condition primarily occurs over th… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100209 |
| Hematoma, Subdural, Acute Accumulation of blood in the SUBDURAL SPACE with acute onset of neurological symptoms. Symptoms may include loss of consciousness, severe HEADACHE, a… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100210 |
| Hematoma, Subdural, Chronic Accumulation of blood in the SUBDURAL SPACE with delayed onset of neurological symptoms. Symptoms may include loss of consciousness, severe HEADACHE,… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100211 |
| Hematoma, Subdural, Intracranial Accumulation of blood in the SUBDURAL SPACE over the CEREBRAL HEMISPHERE. | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100212 |
| Hematoma, Subdural, Spinal Subdural hematoma of the SPINAL CANAL. | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:230147 |
| Hemianopsia Partial or complete loss of vision in one half of the visual field(s) of one or both eyes. Subtypes include altitudinal hemianopsia, characterized by… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100571 |
| Hemiplegia Severe or complete loss of motor function on one side of the body. This condition is usually caused by BRAIN DISEASES that are localized to the cereb… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100533 |
| Hemorrhagic Stroke Stroke due to rupture of a weakened blood vessel in the brain (e.g., CEREBRAL HEMISPHERES; CEREBELLUM; SUBARACHNOID SPACE). | Vascular Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100219 |
| Hereditary Central Nervous System Demyelinating Diseases Inherited conditions characterized by a loss of MYELIN in the central nervous system. | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100081 |
| Hereditary Sensory and Autonomic Neuropathies A group of inherited disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and clinically by loss of sensation and aut… | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100381 |
| Hereditary Sensory and Motor Neuropathy A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both ref… | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100382 |
| Heredodegenerative Disorders, Nervous System Inherited disorders characterized by progressive atrophy and dysfunction of anatomically or physiologically related neurologic systems. | Degenerative Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100415 |
| High Pressure Neurological Syndrome A syndrome related to increased atmospheric pressure and characterized by tremors, nausea, dizziness, decreased motor and mental performance, and SEI… | Syndrome | Pathology | Nervous System [curated_secondary] | AMW:DIS:100303 |
| Hippocampal Sclerosis Neuronal loss in the hippocampal regions of CA1 and CA4 and less severely CA2 and CA3. Additional loss of hippocampal stratum radiatum, hippocampal a… | Degenerative Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100391 |