familial periodic paralysis, nos

Preferred Label : familial periodic paralysis, nos;

Origin ID

D6-98500;

UMLS CUI

C0030443;

Automatic exact mappings (from CISMeF team)
- Familial periodic paralysis [PASCAL descriptor]
- Westphal disease [MeSH concept]
- Westphal disease (disorder) [SNOMED CT concept]
- westphal disease [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Familial Periodic Paralysis [NCIt concept]
- Familial periodic paralysis [MedDRA Preferred Term]
- Familial periodic paralysis (disorder) [SNOMED CT concept]
- Hypokalemic periodic paralysis [ORDO Disease]
- Periodic paralysis [ICD-11 Subcategory]
- hypokalemic periodic paralysis [MeSH Descriptor]
- hypokalemic periodic paralysis [MeSH concept]
- paralyses, familial periodic [MeSH Descriptor]
- paralyses, familial periodic [MeSH concept]
ICD-10 exact mapping(s)
- Periodic paralysis [ICD-10 Sub-category (who)]
Metaterm(s)
- metabolism [CISMeF Metaterm]
- neurology [CISMeF Metaterm]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial Periodic Paralysis [NCIt concept]
- Familial periodic paralysis [MedDRA Preferred Term]
- Familial periodic paralysis (disorder) [SNOMED CT concept]
- Paralysis periodic [MedDRA LLT]
- familial periodic paralyses [Disease (Nov.)]
- familial periodic paralysis [DO Concept]
- paralyses, familial periodic [MeSH Descriptor]
- paralyses, familial periodic [MeSH concept]
Validated automatic mappings to BTNT
- hypokalemic periodic paralysis [Disease (Nov.)]