ONKI3 | Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Paralyses, Familial Periodic

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Metal Metabolism, Inborn Errors ∟ Paralyses, Familial Periodic 28 coordinate concepts 2 subordinate concepts ∟ Hypokalemic Periodic Paralysis \| ∟ Paralysis, Hyperkalemic Periodic ∟ Hemochromatosis \| ∟ Hepatolenticular Degeneration \| ∟ Hypophosphatasia \| ∟ Hypophosphatemia, Familial \| ∟ Menkes Kinky Hair Syndrome \| ∟ Pseudohypoparathyroidism \| ∟ Arthrogryposis \| ∟ Compartment Syndromes \| ∟ Contracture \| ∟ Craniomandibular Disorders \| ∟ Eosinophilia-Myalgia Syndrome \| ∟ Fatigue Syndrome, Chronic \| ∟ Fibromyalgia \| ∟ Isaacs Syndrome \| ∟ Mitochondrial Myopathies \| ∟ Muscle Cramp \| ∟ Muscle Neoplasms \| ∟ Muscle Rigidity \| ∟ Muscle Spasticity \| ∟ Muscle Weakness \| ∟ Muscular Disorders, Atrophic \| ∟ Myofascial Pain Syndromes \| ∟ Myopathies, Structural, Congenital \| ∟ Myositis \| ∟ Myotonic Disorders \| ∟ Polymyalgia Rheumatica \| ∟ Rhabdomyolysis \| ∟ Tendinopathy Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Muscular Diseases ∟ Paralyses, Familial Periodic 28 coordinate concepts 2 subordinate concepts ∟ Hypokalemic Periodic Paralysis \| ∟ Paralysis, Hyperkalemic Periodic ∟ Hemochromatosis \| ∟ Hepatolenticular Degeneration \| ∟ Hypophosphatasia \| ∟ Hypophosphatemia, Familial \| ∟ Menkes Kinky Hair Syndrome \| ∟ Pseudohypoparathyroidism \| ∟ Arthrogryposis \| ∟ Compartment Syndromes \| ∟ Contracture \| ∟ Craniomandibular Disorders \| ∟ Eosinophilia-Myalgia Syndrome \| ∟ Fatigue Syndrome, Chronic \| ∟ Fibromyalgia \| ∟ Isaacs Syndrome \| ∟ Mitochondrial Myopathies \| ∟ Muscle Cramp \| ∟ Muscle Neoplasms \| ∟ Muscle Rigidity \| ∟ Muscle Spasticity \| ∟ Muscle Weakness \| ∟ Muscular Disorders, Atrophic \| ∟ Myofascial Pain Syndromes \| ∟ Myopathies, Structural, Congenital \| ∟ Myositis \| ∟ Myotonic Disorders \| ∟ Polymyalgia Rheumatica \| ∟ Rhabdomyolysis \| ∟ Tendinopathy Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Muscular Diseases ∟ Paralyses, Familial Periodic 28 coordinate concepts 2 subordinate concepts ∟ Hypokalemic Periodic Paralysis \| ∟ Paralysis, Hyperkalemic Periodic ∟ Hemochromatosis \| ∟ Hepatolenticular Degeneration \| ∟ Hypophosphatasia \| ∟ Hypophosphatemia, Familial \| ∟ Menkes Kinky Hair Syndrome \| ∟ Pseudohypoparathyroidism \| ∟ Arthrogryposis \| ∟ Compartment Syndromes \| ∟ Contracture \| ∟ Craniomandibular Disorders \| ∟ Eosinophilia-Myalgia Syndrome \| ∟ Fatigue Syndrome, Chronic \| ∟ Fibromyalgia \| ∟ Isaacs Syndrome \| ∟ Mitochondrial Myopathies \| ∟ Muscle Cramp \| ∟ Muscle Neoplasms \| ∟ Muscle Rigidity \| ∟ Muscle Spasticity \| ∟ Muscle Weakness \| ∟ Muscular Disorders, Atrophic \| ∟ Myofascial Pain Syndromes \| ∟ Myopathies, Structural, Congenital \| ∟ Myositis \| ∟ Myotonic Disorders \| ∟ Polymyalgia Rheumatica \| ∟ Rhabdomyolysis \| ∟ Tendinopathy Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Metal Metabolism, Inborn Errors ∟ Paralyses, Familial Periodic 28 coordinate concepts 2 subordinate concepts ∟ Hypokalemic Periodic Paralysis \| ∟ Paralysis, Hyperkalemic Periodic ∟ Hemochromatosis \| ∟ Hepatolenticular Degeneration \| ∟ Hypophosphatasia \| ∟ Hypophosphatemia, Familial \| ∟ Menkes Kinky Hair Syndrome \| ∟ Pseudohypoparathyroidism \| ∟ Arthrogryposis \| ∟ Compartment Syndromes \| ∟ Contracture \| ∟ Craniomandibular Disorders \| ∟ Eosinophilia-Myalgia Syndrome \| ∟ Fatigue Syndrome, Chronic \| ∟ Fibromyalgia \| ∟ Isaacs Syndrome \| ∟ Mitochondrial Myopathies \| ∟ Muscle Cramp \| ∟ Muscle Neoplasms \| ∟ Muscle Rigidity \| ∟ Muscle Spasticity \| ∟ Muscle Weakness \| ∟ Muscular Disorders, Atrophic \| ∟ Myofascial Pain Syndromes \| ∟ Myopathies, Structural, Congenital \| ∟ Myositis \| ∟ Myotonic Disorders \| ∟ Polymyalgia Rheumatica \| ∟ Rhabdomyolysis \| ∟ Tendinopathy X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Metal Metabolism, Inborn Errors ∟ Paralyses, Familial Periodic Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Muscular Diseases ∟ Paralyses, Familial Periodic Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Muscular Diseases ∟ Paralyses, Familial Periodic Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Metal Metabolism, Inborn Errors ∟ Paralyses, Familial Periodic Metal Metabolism, Inborn Errors > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Muscular Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) Muscular Diseases > Neuromuscular Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Metal Metabolism, Inborn Errors > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Hypokalemic Periodic Paralysis \| Paralysis, Hyperkalemic Periodic X
Annotation:	a specific disease entity: see MeSH definition X
historyNote*:	2000(1966) X
publicMeSHNote*:	2000; see PARALYSIS, FAMILIAL PERIODIC 1966-1999 X
Scope note:	A heterogenous group of inherited disorders characterized by recurring attacks of rapidly progressive flaccid paralysis or myotonia. These conditions have in common a mutation of the gene encoding the alpha subunit of the sodium channel in skeletal muscle. They are frequently associated with fluctuations in serum potassium levels. Periodic paralysis may also occur as a non-familial process secondary to THYROTOXICOSIS and other conditions. (From Adams et al., Principles of Neurology, 6th ed, p1481) X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Hemochromatosis \| Hepatolenticular Degeneration \| Hypophosphatasia \| Hypophosphatemia, Familial \| Menkes Kinky Hair Syndrome \| Pseudohypoparathyroidism \| Arthrogryposis \| Compartment Syndromes \| Contracture \| Craniomandibular Disorders \| Eosinophilia-Myalgia Syndrome \| Fatigue Syndrome, Chronic \| Fibromyalgia \| Isaacs Syndrome \| Mitochondrial Myopathies \| Muscle Cramp \| Muscle Neoplasms \| Muscle Rigidity \| Muscle Spasticity \| Muscle Weakness \| Muscular Disorders, Atrophic \| Myofascial Pain Syndromes \| Myopathies, Structural, Congenital \| Myositis \| Myotonic Disorders \| Polymyalgia Rheumatica \| Rhabdomyolysis \| Tendinopathy X
URI:	X
Labels and equivalent concepts:	Familiaaliset periodiset paralyysit (fi) Suvuittaiset periodiset paralyysit (fi, replaced) Suvuittainen periodinen pareesi (fi, replaced) Suvuittaiset periodiset pareesit (fi, replaced) Velttohalvauskohtaukset (fi, replaced) Velttohalvauskohtaus (fi, replaced) Suvuittainen periodinen paralyysi (fi, replaced) Periodiset paralyysit (fi, replaced) Ajoittainen velttohalvaus (fi, replaced) Ajoittaiset velttohalvaukset (fi, replaced) Familiaaliset periodiset pareesit (fi, replaced) Periodinen paralyysi (fi, replaced) Paralyser, familjära periodiska (sv) Periodiska familjära paralyser (sv, replaced) Periodic Paralysis, Familial (en, replaced) Familial Periodic Paralysis (en, replaced) X
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