Orphanet: Genetic primary hypomagnesemia
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Genetic primary hypomagnesemia

Disease definition

A rare mineral absorption and transport disorder characterized by a selective defect in renal or intestinal magnesium (Mg) absorption, resulting in a low Mg concentration in the blood.

ORPHA:34526

Classification level: Group of disorders
  • Synonym(s): -
  • Prevalence: Unknown
  • Inheritance: Autosomal dominant or Autosomal recessive 
  • Age of onset: Childhood, Adolescent, Adult
  • ICD-10: E83.4
  • OMIM: -
  • UMLS: -
  • MeSH: -
  • GARD: 2906
  • MedDRA: -

Detailed information

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