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Diseases / Metabolic disease/ Inborn errors of metabolism/ Inborn metal metabolism disorder/ Familial primary hypomagnesemia/ Familial primary hypomagnesemia with normocalcuria/ Familial primary hypomagnesemia with normocalciuria and normocalcemia

Hypomagnesemia, seizures, and intellectual disability

rare

Identifiers: MONDO:0014631
Part of: Familial primary hypomagnesemia with normocalciuria and normocalcemia
Also known as: HOMGSMR · hypomagnesemia, seizures, and mental retardation

Subtypes

All diseases Rare only

Disease

Hypomagnesemia, seizures, and intellectual disability 1 MONDO:0020787 CNNM2
Hypomagnesemia, seizures, and intellectual disability 2 MONDO:0020788 ATP1A1

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