loading...| Preferred Name | Hypokalemic Periodic Paralysis [Disease/Finding] | |
| Synonyms |
Periodic Paralysis- Hypokalemic Familial Hypokalemic Periodic Paralysis Paralysis, Hypokalemic Periodic HYPOKPP Westphall Disease HOKPP Hypokalemic Periodic Paralysis, Familial Hypokalemic Periodic Paralysis HYPOPP Primary Hypokalemic Periodic Paralysis |
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| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000004156 |
|
| altLabel |
Periodic Paralysis- Hypokalemic Familial Hypokalemic Periodic Paralysis Paralysis, Hypokalemic Periodic HYPOKPP Westphall Disease HOKPP Hypokalemic Periodic Paralysis, Familial Hypokalemic Periodic Paralysis HYPOPP Primary Hypokalemic Periodic Paralysis |
|
| cui |
C0238358 |
|
| MESH DEFINITION |
An autosomal dominant familial disorder characterized by recurrent episodes of skeletal muscle weakness associated with falls in serum potassium levels. The condition usually presents in the first or second decade of life with attacks of trunk and leg paresis during sleep or shortly after awakening. Symptoms may persist for hours to days and generally are precipitated by exercise or a meal high in carbohydrates. (Adams et al., Principles of Neurology, 6th ed, p1483) |
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| MESH DUI |
D020514 |
|
| MeSH name |
Hypokalemic Periodic Paralysis |
|
| MESH UI |
M0328337 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000004156 |
|
| NUI |
N0000004156 |
|
| prefLabel |
Hypokalemic Periodic Paralysis [Disease/Finding] |
|
| SNOMED CID |
240093008 82732003 |
|
| tui |
T047 |
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| subClassOf |