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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 |
|---|---|---|---|---|
| Muscle Hypertonia Abnormal increase in skeletal or smooth muscle tone. Skeletal muscle hypertonicity may be associated with PYRAMIDAL TRACT lesions or BASAL GANGLIA DI… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100523 |
| Muscle Hypotonia A diminution of the skeletal muscle tone marked by a diminished resistance to passive stretching. | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100524 |
| Muscular Atrophy Derangement in size and number of muscle fibers occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessnes… | Degenerative Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100525 |
| Muscular Atrophy, Spinal A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually witho… | Degenerative Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100319 |
| Myasthenia Gravis, Autoimmune, Experimental Any autoimmune animal disease model used in the study of MYASTHENIA GRAVIS. Injection with purified neuromuscular junction acetylcholine receptor (AC… | Immune Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100013 |
| Myasthenia Gravis, Neonatal A disorder of neuromuscular transmission that occurs in a minority of newborns born to women with myasthenia gravis. Clinical features are usually pr… | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100014 |
| Myasthenic Syndromes, Congenital A heterogeneous group of disorders characterized by a congenital defect in neuromuscular transmission at the NEUROMUSCULAR JUNCTION. This includes pr… | Syndrome | Pathology | Nervous System [curated_secondary] | AMW:DIS:100578 |
| Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease A disease in which serum antibodies are directed against MYELIN-OLIGODENDROCYTE GLYCOPROTEIN. MOGAD is typically associated with ACUTE DISSEMINATED E… | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100011 |
| Myelinolysis, Central Pontine A demyelinating condition affecting the PONS and characterized clinically by an acute progressive QUADRIPLEGIA; DYSARTHRIA; DYSPHAGIA; and alteration… | Metabolic Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100132 |
| Myoclonic Cerebellar Dyssynergia A condition marked by progressive CEREBELLAR ATAXIA combined with MYOCLONUS usually presenting in the third decade of life or later. Additional clini… | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100161 |
| Myoclonic Epilepsies, Progressive A heterogeneous group of primarily familial EPILEPSY disorders characterized by myoclonic seizures, tonic-clonic seizures, ataxia, progressive intell… | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100251 |
| Myoclonic Epilepsy, Juvenile A disorder characterized by the onset of myoclonus in adolescence, a marked increase in the incidence of absence seizures (see EPILEPSY, ABSENCE), an… | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100254 |
| Myoclonus Involuntary shock-like contractions, irregular in rhythm and amplitude, followed by relaxation, of a muscle or a group of muscles. This condition may… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100442 |
| Myokymia Successive and rapid contractions of motor units associated with chronic nerve injury. The discharges arise from the peripheral aspects of regenerati… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100527 |
| Myotonia Prolonged failure of muscle relaxation after contraction. This may occur after voluntary contractions, muscle percussion, or electrical stimulation o… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100528 |
| Narcolepsy A condition characterized by recurrent episodes of daytime somnolence and lapses in consciousness (microsomnias) that may be associated with automati… | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100637 |
| Neonatal Brachial Plexus Palsy Perinatal nerve injury involving the BRACHIAL PLEXUS involving a weak or paralyzed upper extremity. | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100584 |
| Nerve Compression Syndromes Mechanical compression of nerves or nerve roots from internal or external causes. These may result in a conduction block to nerve impulses (due to MY… | Syndrome | Pathology | Nervous System [curated_secondary] | AMW:DIS:100601 |
| Nervous System Autoimmune Disease, Experimental Experimental animal models for human AUTOIMMUNE DISEASES OF THE NERVOUS SYSTEM. They include GUILLAIN-BARRE SYNDROME (see NEURITIS, AUTOIMMUNE, EXPER… | Immune Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100015 |
| Nervous System Diseases Diseases of the central and peripheral nervous system. This includes disorders of the brain, spinal cord, cranial nerves, peripheral nerves, nerve ro… | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100001 |
| Nervous System Malformations Structural abnormalities of the central or peripheral nervous system resulting primarily from defects of embryogenesis. | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100375 |
| Neural Tube Defects Congenital malformations of the central nervous system and adjacent structures related to defective neural tube closure during the first trimester of… | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100401 |
| Neuralgia Intense or aching pain that occurs along the course or distribution of a peripheral or cranial nerve. | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100606 |
| Neuralgia, Postherpetic Pain in nerves, frequently involving facial SKIN, resulting from the activation the latent varicella-zoster virus (HERPESVIRUS 3, HUMAN). The two for… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100607 |
| Neuritis A general term indicating inflammation of a peripheral or cranial nerve. Clinical manifestation may include PAIN; PARESTHESIAS; PARESIS; or HYPESTHES… | Inflammatory Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100608 |
| Neuritis, Autoimmune, Experimental An experimental animal model for the demyelinating disease of GUILLAINE-BARRE SYNDROME. In the most frequently used protocol, animals are injected wi… | Immune Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100017 |
| Neuroacanthocytosis An inherited autosomal disorder that is characterized by neurodegeneration; orofacial and buccal DYSKINESIAS; CHOREA; and thorny-looking red cells (A… | Congenital Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100310 |
| Neuroaxonal Dystrophies A nonspecific term referring both to the pathologic finding of swelling of distal portions of axons in the brain and to disorders which feature this … | Disorder | Pathology | Nervous System [curated_secondary] | AMW:DIS:100300 |
| Neurobehavioral Manifestations Signs and symptoms of higher cortical dysfunction caused by organic conditions. These include certain behavioral alterations and impairments of skill… | Pathologic Condition | Pathology | Nervous System [curated_secondary] | AMW:DIS:100450 |
| Neurocutaneous Syndromes A group of disorders characterized by ectodermal-based malformations and neoplastic growths in the skin, nervous system, and other organs. | Syndrome | Pathology | Nervous System [curated_secondary] | AMW:DIS:100412 |