Agent Commons Collaborative Research

Familial primary hypomagnesemia

rare

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

Identifiers
MONDO:0018100 Orphanet:34526
Part of
Disorder of magnesium transportInborn metal metabolism disorderInherited renal tubular disease

Subtypes

All diseases Rare only
Disease Subtypes
Familial primary hypomagnesemia with normocalcuria 8
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis 2
Familial primary hypomagnesemia with hypocalcuria 1
EGF-related primary hypomagnesemia with intellectual disability
Hypomagnesemia 7, renal, with or without dilated cardiomyopathy

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