familial hypokalemia-hypomagnesemia

Preferred Label : familial hypokalemia-hypomagnesemia;

Details

Origin ID

D6-98720;

UMLS CUI

C0268450;

Currated CISMeF NLP mapping
- Familial hypokalaemia - hypomagnesaemia [ICD-11 More detail]
- Familial hypokalemia-hypomagnesemia (disorder) [Inactive SNOMED CT concept]
- Gitelman Syndrome [NCIt concept]
- Gitelman syndrome [PASCAL descriptor]
- Gitelman syndrome [Disease (Nov.)]
- Gitelman syndrome [DO Concept]
- Gitelman syndrome [ORDO Disease]
- Gitelman syndrome [OMIM Phenotype]
- Gitelman syndrome (disorder) [SNOMED CT concept]
- Gitelman's syndrome [MedDRA Preferred Term]
- gitelman syndrome [MeSH Descriptor]
- gitelman syndrome [MeSH concept]
ICD-10 exact mapping(s)
- Other disorders of mineral metabolism [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Genetic primary hypomagnesemia [ORDO Disease]
Metaterm(s)
- metabolism [CISMeF Metaterm]
SNOMED CT concept
- Familial hypokalemia-hypomagnesemia (disorder) [Inactive SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial hypokalaemia - hypomagnesaemia [ICD-11 More detail]
- Familial hypokalemia-hypomagnesemia (disorder) [Inactive SNOMED CT concept]
- Gitelman Syndrome [NCIt concept]
- Gitelman syndrome [ORDO Disease]
- Gitelman syndrome [OMIM Phenotype]
- Gitelman syndrome [Disease (Nov.)]
- Gitelman syndrome [DO Concept]
- Gitelman syndrome [PASCAL descriptor]
- Gitelman syndrome (disorder) [SNOMED CT concept]
- Gitelman's syndrome [MedDRA Preferred Term]
- gitelman syndrome [MeSH concept]
- gitelman syndrome [MeSH Descriptor]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients