Hypokalemic Periodic Paralysis

Preferred Label : Hypokalemic Periodic Paralysis;

NCIt definition : A rare, autosomal dominant inherited disorder characterized by irregular episodes of muscle weakness or paralysis which are always accompanied by low levels of potassium in the blood.;

Details

Origin ID

C84775;

UMLS CUI

C0238358;

Currated CISMeF NLP mapping
- Familial hypokalemic periodic paralysis (disorder) [SNOMED CT concept]
- Familial periodic paralysis [MedDRA Preferred Term]
- Hypokalaemic periodic paralysis [MedDRA LLT]
- Hypokalaemic periodic paralysis [ICD-11 Sub-sub category]
- Hypokalemic periodic paralysis [MedDRA LLT]
- Hypokalemic periodic paralysis [ORDO Disease]
- Hypokalemic periodic paralysis (disorder) [Inactive SNOMED CT concept]
- Hypokalemic periodic paralysis, type 1 [OMIM Phenotype]
- familial hypokalemic periodic paralysis [SNOMED Notion]
- hypokalemic periodic paralysis [DO Concept]
- hypokalemic periodic paralysis [Disease (Nov.)]
- hypokalemic periodic paralysis [MeSH Descriptor]
- hypokalemic periodic paralysis [MeSH concept]
- paralysis, hyperkalemic periodic [MeSH concept]
- paralysis, hyperkalemic periodic [MeSH Descriptor]
DO Cross reference
- hypokalemic periodic paralysis [DO Concept]
See also inter- (CISMeF)
- hyperkalemic periodic paralysis [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial hypokalemic periodic paralysis (disorder) [SNOMED CT concept]
- Hypokalaemic periodic paralysis [MedDRA LLT]
- Hypokalemic periodic paralysis [MedDRA LLT]
- Hypokalemic periodic paralysis (disorder) [Inactive SNOMED CT concept]
- familial hypokalemic periodic paralysis [SNOMED Notion]
- hypokalemic periodic paralysis [DO Concept]
- hypokalemic periodic paralysis [MeSH concept]
- hypokalemic periodic paralysis [MeSH Descriptor]
disease_has_finding
- Rare Lesion [NCIt concept]

Keyword's position in hierarchy(ies) :

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