renal hypomagnesemia 2 (Q32136745)

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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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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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