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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 |
|---|---|---|---|---|
| Trochlear Nerve Injuries Traumatic injuries to the TROCHLEAR NERVE. | Traumatic Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100347 |
| Tyrosinemias A group of disorders which have in common elevations of tyrosine in the blood and urine secondary to an enzyme deficiency. Type I tyrosinemia feature… | Congenital Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100123 |
| Ulnar Nerve Compression Syndromes Ulnar neuropathies caused by mechanical compression of the nerve at any location from its origin at the BRACHIAL PLEXUS to its terminations in the ha… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100600 |
| Ulnar Neuropathies Disease involving the ULNAR NERVE from its origin in the BRACHIAL PLEXUS to its termination in the hand. Clinical manifestations may include PARESIS … | Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100598 |
| Unconsciousness Loss of the ability to maintain awareness of self and environment combined with markedly reduced responsiveness to environmental stimuli. (From Adams… | Pathologic Condition | Pathology | Neurology [curated_secondary] | AMW:DIS:100479 |
| Unverricht-Lundborg Syndrome An autosomal recessive condition characterized by recurrent myoclonic and generalized seizures, ATAXIA, slowly progressive intellectual deterioration… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100253 |
| Urea Cycle Disorders, Inborn Rare congenital metabolism disorders of the urea cycle. The disorders are due to mutations that result in complete (neonatal onset) or partial (child… | Congenital Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100124 |
| Urinary Bladder, Neurogenic Dysfunction of the URINARY BLADDER due to disease of the central or peripheral nervous system pathways involved in the control of URINATION. This is … | Pathologic Condition | Pathology | Neurology [curated_secondary] | AMW:DIS:100575 |
| Uveomeningoencephalitic Syndrome A syndrome characterized by bilateral granulomatous UVEITIS with IRITIS and secondary GLAUCOMA, premature ALOPECIA, symmetrical VITILIGO, poliosis ci… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100023 |
| Vagus Nerve Diseases Diseases of the tenth cranial nerve, including brain stem lesions involving its nuclei (solitary, ambiguus, and dorsal motor), nerve fascicles, and i… | Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100373 |
| Vagus Nerve Injuries Traumatic injuries to the VAGUS NERVE. Because the vagus nerve innervates multiple organs, injuries in the nerve fibers may result in any gastrointes… | Traumatic Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100348 |
| Vasculitis, Central Nervous System Inflammation of blood vessels within the central nervous system. Primary vasculitis is usually caused by autoimmune or idiopathic factors, while seco… | Vascular Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100024 |
| Vasospasm, Intracranial Constriction of arteries in the SKULL due to sudden, sharp, and often persistent smooth muscle contraction in blood vessels. Intracranial vasospasm r… | Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100225 |
| Vein of Galen Malformations Congenital arteriovenous malformation involving the VEIN OF GALEN, a large deep vein at the base of the brain. The rush of arterial blood directly in… | Congenital Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100196 |
| Vertebral Artery Dissection Splitting of the vessel wall in the VERTEBRAL ARTERY. Interstitial hemorrhage into the media of the vessel wall can lead to occlusion of the vertebra… | Traumatic Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100188 |
| Vertebrobasilar Insufficiency Localized or diffuse reduction in blood flow through the vertebrobasilar arterial system, which supplies the BRAIN STEM; CEREBELLUM; OCCIPITAL LOBE; … | Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100175 |
| Vision Disorders Visual impairments limiting one or more of the basic functions of the eye: visual acuity, dark adaptation, color vision, or peripheral vision. These … | Pathologic Condition | Pathology | Neurology [curated_secondary] | AMW:DIS:100565 |
| Vision, Low Vision considered to be inferior to normal vision as represented by accepted standards of acuity, field of vision, or motility. Low vision generally … | Pathologic Condition | Pathology | Neurology [curated_secondary] | AMW:DIS:100574 |
| von Hippel-Lindau Disease An autosomal dominant disorder caused by mutations in a tumor suppressor gene. This syndrome is characterized by abnormal growth of small blood vesse… | Congenital Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100413 |
| Walker-Warburg Syndrome Rare autosomal recessive lissencephaly type 2 associated with congenital MUSCULAR DYSTROPHY and eye anomalies (e.g., RETINAL DETACHMENT; CATARACT; MI… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100396 |
| Wernicke Encephalopathy An acute neurological disorder characterized by the triad of ophthalmoplegia, ataxia, and disturbances of mental activity or consciousness. Eye movem… | Metabolic Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100133 |
| Williams Syndrome A disorder caused by hemizygous microdeletion of about 28 genes on chromosome 7q11.23, including the ELASTIN gene. Clinical manifestations include SU… | Syndrome | Pathology | Neurology [curated_secondary] | AMW:DIS:100497 |
| X-Linked Emery-Dreifuss Muscular Dystrophy Emery-Dreifuss muscular dystrophy associated with mutations on emerin (EMD gene) or four and a half LIM domains 1 (FHL1 gene) both located on X chrom… | Congenital Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:050272 |
| X-Linked Intellectual Disability A class of genetic disorders resulting in INTELLECTUAL DISABILITY that is associated either with mutations of GENES located on the X CHROMOSOME or ab… | Congenital Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100489 |
| Zygomatic Fractures Fractures of the zygoma. | Traumatic Disorder | Pathology | Neurology [curated_secondary] | AMW:DIS:100667 |