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Summary Literature (0)
DOID:0060885 - renal hypomagnesemia 2

Disease Ontology Definition:A hypomagnesemia characterized by autosomal dominant inheritance of hypomagnesemia due to renal magnesium loss that has_material_basis_in heterozygous mutation in the FXYD2 gene on chromosome 11q23.

Synonyms: autosomal dominant primary hypomagnesemia with hypocalciuria, HOMG2

Xenbase Genes : fxyd2, hnf1b

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007937 - renal hypomagnesemia 2

MIM:
MIM:154020 - HYPOMAGNESEMIA 2, RENAL; HOMG2

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

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