Term Name:	renal hypomagnesemia 2
Synonyms:	autosomal dominant primary hypomagnesemia with hypocalciuria, HOMG2
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.
Ontology:	Human Disease [DOID:0060885]   ( DOID:0060885 )