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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
Hypomagnesemia 7, renal, with or without dilated cardiomyopathy
rare
Identifiers
MONDO:0859328
OMIM:620152
Causal genes
RRAGD
Part of
Familial primary hypomagnesemia
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