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ENHypomagnesemia 2, Renal (HOMG2)
Alias:
Renal Hypomagnesemia 2
Homg2
Autosomal Dominant Primary Hypomagnesemia with Hypocalciuria
Isolated Autosomal Dominant Hypomagnesemia
Isolated Renal Magnesium Wasting
Renal Hypomagnesemia Type 2
Magnesium Wasting, Renal
Hypomagnesemia with Hypocalciuria
Magnesium Loss, Isolated Renal
Renal Hypomagnesemia, Dominant
Dominant Renal Hypomagnesemia
Isolated Renal Magnesium Loss
Hypomagnesemia, Type 2, Renal
Magnesium Wasting Renal
Renal Magnesium Wasting
Hypomagnesemia-2, Renal
Hypomagnesemia 2
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Hypomagnesemia 2, Renal, also known as renal hypomagnesemia 2, is related to hypomagnesemia 3, renal and gitelman syndrome, and has symptoms including seizures and weakness. An important gene associated with Hypomagnesemia 2, Renal is FXYD2 (FXYD Domain Containing Ion Transport Regulator 2), and among its related pathways/superpathways are Infectious disease and Transport of inorganic cations/anions and amino acids/oligopeptides. Affiliated tissues include kidney and skeletal muscle, and related phenotypes are renal insufficiency and hypomagnesemia
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MALACARDS
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MGI
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IF
