KEGG   DISEASE: H01210Help
Entry
H01210                      Disease                                
Name
Hypomagnesemia
Description
Hypomagnesemia is defined as a serum magnesium level less than 1.8 mg/dl. Hypomagnesemia may result from inadequate magnesium intake, increased gastrointestinal or renal losses, or redistribution from extracellular to intracellular space.
Category
Inherited metabolic disease
BRITE hierarchy
Pathway
hsa04978 Mineral absorption  
 
Focal adhesion
Cell adhesion molecules (CAMs)
Tight junction
Gap junction
Gene
TRPM6 [HSA:140803] [KO:K04981]
FXYD2 [HSA:486] [KO:K01538]
CLDN16 [HSA:10686] [KO:K06087]
EGF [HSA:1950] [KO:K04357]
CLDN19 [HSA:149461] [KO:K06087]
Env factor
Furosemide [DR:D00331]
Drug
Magnesium oxide [DR:D01167]
Magnesium sulfate heptahydrate [DR:D01108]
Comment
Gitelman syndrome is described in H00240. [DS:H00240]
Other DBs
Reference
  Authors
Assadi F
  Title
Hypomagnesemia: an evidence-based approach to clinical cases.
  Journal
Iran J Kidney Dis 4:13-9 (2010)

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