manz syndrome - CISMeF

Preferred Label : manz syndrome;

MeSH note : Polyuria, nystagmus and recurrent episodes of tetany with radiological evidence of rickets and nephrocalcinosis;

MeSH synonym : familial hypomagnesemia - hypercalciuria;

Details

Origin ID

C535709;

UMLS CUI

C0268451;

Automatic exact mappings (from CISMeF team)
- Familial hypomagnesemia-hypercalciuria (disorder) [SNOMED CT concept]
- familial hypomagnesemia-hypercalciuria [SNOMED Notion]
MeSH term(s) associated for indexing
- magnesium deficiency [MeSH Descriptor]
- nephrocalcinosis [MeSH Descriptor]
Record concept(s)
- Manz syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial hypomagnesemia-hypercalciuria (disorder) [SNOMED CT concept]
- familial hypomagnesemia-hypercalciuria [SNOMED Notion]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients