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bn:02721836n
Noun Concept
Categories: Rare diseases, Channelopathies, Myoneural junction and neuromuscular diseases
EN
hypokalemic periodic paralysis  familial hypokalemic periodic paralysis  familial periodic paralysis  HOKPP  Hypokalaemic familial periodic paralysis
EN
Hypokalemic periodic paralysis, also known as familial hypokalemic periodic paralysis, is a rare, autosomal dominant channelopathy characterized by muscle weakness or paralysis when there is a fall in potassium levels in the blood. Wikipedia
Definitions
Relations
Sources
EN
Hypokalemic periodic paralysis, also known as familial hypokalemic periodic paralysis, is a rare, autosomal dominant channelopathy characterized by muscle weakness or paralysis when there is a fall in potassium levels in the blood. Wikipedia
A muscle disease Wikipedia Disambiguation
Human disease Wikidata
IS A
rare disease
channelopathy
periodic paralysis
DRUG USED FOR TREATMENT
diclofenamide
GENETIC ASSOCIATION
CACNA1S
Nav1.4
HAS CAUSE
mutation
HEALTH SPECIALTY
neurology
neuromuscular medicine
MEDICAL EXAMINATIONS
electromyography
genetic screening
muscle biopsy
POSSIBLE TREATMENT
potassium chloride
SYMPTOMS
hypokalemia
myasthenia
Wikipedia
EN
hypokalemic periodic paralysis
Wikidata
EN
hypokalemic periodic paralysis
Wikipedia Redirections
EN
familial hypokalemic periodic paralysis, HOKPP, Hypokalaemic familial periodic paralysis, hypokalaemic periodic paralysis, Hypokalemic periodic paralysis type 1, hypoKPP, HypoPP, Primary Hypokalemic Periodic Paralysis, Westphall disease
Wikidata Alias
EN
familial hypokalemic periodic paralysis, familial periodic paralysis, HOKPP, Hypokalemic familial periodic paralysis, Hypokalemic periodic paralysis, periodic hypokalemic paralysis, Periodic paralysis I, Westphal disease

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