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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
| Id | http://purl.bioontology.org/ontology/NDFRT/N0000002305
http://purl.bioontology.org/ontology/NDFRT/N0000002305
|
|---|---|
| Preferred Name | Paralyses, Familial Periodic [Disease/Finding] |
| Synonyms |
Familial Periodic Paralysis
Paralyses, Familial Periodic
Periodic Paralysis, Familial
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
Familial Periodic Paralysis
Paralyses, Familial Periodic
Periodic Paralysis, Familial
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|---|---|
| prefLabel | Paralyses, Familial Periodic [Disease/Finding]
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| MESH DEFINITION | 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)
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| MESH DUI | D010245
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| MESH UI | M0015880
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| MeSH name | Paralyses, Familial Periodic
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| type | |
| tui | T047
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| SNOMED CID | 267607008
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| notation | N0000002305
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| Semantic type UMLS property | |
| NUI | N0000002305
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| cui | C0030443
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| NDFRT kind | DISEASE_KIND
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| subClassOf |
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| No notes to display |