Normokalemic periodic paralysis

Preferred Label : Normokalemic periodic paralysis;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 170600;

Details

Origin ID

170600;

UMLS CUI

C0268445;

Automatic exact mappings (from CISMeF team)
- Normokalaemic periodic paralysis [ICD-11 More detail]
- paralyses, familial periodic [MeSH Descriptor]
Currated CISMeF NLP mapping
- Familial normokalemic periodic paralysis (disorder) [SNOMED CT concept]
- Normokalemic Periodic Paralysis [NCIt concept]
- Normokalemic periodic paralysis [ORDO Disease]
- familial normokalemic periodic paralysis [SNOMED Notion]
- normokalemic periodic paralysis [Disease (Nov.)]
- normokalemic periodic paralysis [MeSH concept]
- normokalemic periodic paralysis, Potassium-Sensitive [MeSH Supplementary Concept]
- normokalemic periodic paralysis, Potassium-Sensitive [MeSH concept]
HPO term(s)
- Abnormality of the tongue [HPO term]
- Autosomal dominant inheritance [HPO term]
- Myotonia [HPO term]
- Periodic paralysis [HPO term]
Not associated HPO term(s)
- Abnormal blood potassium concentration [HPO term]
ORDO concept(s)
- Normokalemic periodic paralysis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial normokalemic periodic paralysis (disorder) [SNOMED CT concept]
- Normokalemic Periodic Paralysis [NCIt concept]
- Normokalemic periodic paralysis [ORDO Disease]
- familial normokalemic periodic paralysis [SNOMED Notion]
- normokalemic periodic paralysis [MeSH concept]

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