familial hypomagnesemia-hypercalciuria

Preferred Label : familial hypomagnesemia-hypercalciuria;

Origin ID

D6-98730;

UMLS CUI

C0268451;

Automatic exact mappings (from CISMeF team)
- Manz syndrome [MeSH concept]
- manz syndrome [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Familial hypomagnesemia-hypercalciuria (disorder) [SNOMED CT concept]
ICD-10 exact mapping(s)
- Other disorders of mineral metabolism [ICD-10 Sub-category (who)]
Metaterm(s)
- metabolism [CISMeF Metaterm]
SNOMED CT concept
- Familial hypomagnesemia-hypercalciuria (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial hypomagnesemia-hypercalciuria (disorder) [SNOMED CT concept]
- Manz syndrome [MeSH concept]
- manz syndrome [MeSH Supplementary Concept]