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Summary Literature (0)
DOID:0060883 - intestinal hypomagnesemia 1

Disease Ontology Definition:A hypomagnesemia characterized by very low serum magnesium levels due to defects in intestinal absorption and kidney excretion and secondary hypocalcemia that has_material_basis_in homozygous or compound heterozygous mutations in the TRPM6 gene on chromosome 9q21.

Synonyms: HOMG1, hypomagnesemia caused by selective magnesium malabsorption, hypomagnesemia intestinal type 1, hypomagnesemic tetany, intestinal hypomagnesemia with secondary hypocalcemia, primary hypomagnesemia with secondary hypocalcemia

Xenbase Genes : trpm6

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011176 - intestinal hypomagnesemia 1

MIM:
MIM:602014 - HYPOMAGNESEMIA 1, INTESTINAL; HOMG1

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)