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Summary Literature (0)
MIM:616418 - HYPOMAGNESEMIA, SEIZURES, AND IMPAIRED INTELLECTUAL DEVELOPMENT 1; HOMGSMR1

Xenbase Genes: cnnm2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018101 - familial primary hypomagnesemia with normocalciuria and normocalcemia
MONDO:0020787 - hypomagnesemia, seizures, and intellectual disability 1