Familial Primary Hypomagnesemia

Preferred Label : Familial Primary Hypomagnesemia;

Alternative definition : NICHD: A hereditary disorder that leads to a selective defect in renal or intestinal magnesium absorption, resulting in a low serum magnesium concentration.;

Details

Origin ID

C123263;

UMLS CUI

C4049202;

Automatic exact mappings (from CISMeF team)
- Genetic primary hypomagnesemia [ORDO Disease]
- Primary familial hypomagnesaemia [MedDRA Preferred Term]
- Primary familial hypomagnesemia [MedDRA LLT]
- primary hypomagnesemia [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Primary familial hypomagnesaemia [MedDRA Preferred Term]
- Primary familial hypomagnesemia [MedDRA LLT]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Nephrology Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

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