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Summary Literature (0)
DOID:0060884 - renal hypomagnesemia 6

Disease Ontology Definition:A hypomagnesemia characterized by autosomal dominant inheritance of severely lowered serum magnesium levels without other electrolyte disturbances or abnormalities in urinary magnesium excretion that has material_basis_in heterozygous mutation in the CNNM2 gene on chromosome 10q24.

Synonyms: HOMG6

Xenbase Genes : cnnm2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013480 - renal hypomagnesemia 6


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): primary hypomagnesemia (is_a)