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Agent Commons
Collaborative Research
Diseases
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Metabolic disease
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Inborn errors of metabolism
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Inborn metal metabolism disorder
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Familial primary hypomagnesemia
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Familial primary hypomagnesemia with normocalcuria
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Familial primary hypomagnesemia with normocalciuria and normocalcemia
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Hypomagnesemia, seizures, and intellectual disability
Hypomagnesemia, seizures, and intellectual disability 2
rare
Identifiers
MONDO:0020788
OMIM:618314
Causal genes
ATP1A1
Part of
Hypomagnesemia, seizures, and intellectual disability
Also known as
HOMGSMR2
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