(Q32136745)
English
renal hypomagnesemia 2
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
- autosomal dominant primary hypomagnesemia with hypocalciuria
- HOMG2
- renal hypomagnesemia type 2
- HYPOMAGNESEMIA 2, RENAL
- Magnesium Loss, Isolated Renal
- Magnesium Wasting, Renal
- Isolated renal magnesium wasting
- HYPOMAGNESEMIA 2, RENAL; HOMG2
- Isolated autosomal dominant hypomagnesemia
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