World Of Taxonomy
C123263Level 4

Familial Primary Hypomagnesemia

**Semantic type:** Disease or Syndrome

**Definition:** A hereditary disorder that leads to a selective defect in renal or intestinal magnesium absorption, resulting in a low serum magnesium concentration.

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C123263 - Familial Primary Hypomagnesemia - NCI Thesaurus - World Of Taxonomy | World Of Taxonomy