Human genes for renal hypomagnesemia 2
Renal hypomagnesemia 2 [DOID:0060885]
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: renal hypomagnesemia 2, DOID:0060885, autosomal dominant primary hypomagnesemia with hypocalciuria, HOMG2, autosomal dominant primary hypomagnesemia with hypocalciurias