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Summary Literature (0)
MIM:613882 - HYPOMAGNESEMIA 6, RENAL; HOMG6

Xenbase Genes: cnnm2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013480 - renal hypomagnesemia 6
MONDO:0018101 - familial primary hypomagnesemia with normocalciuria and normocalcemia

Disease Ontology (DO):
DOID:0060884 - renal hypomagnesemia 6