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
Human diseases [BR:br08402]
 Congenital disorders of metabolism
  Other congenital disorders of metabolism
   H01210  Hypomagnesemia
Human diseases in ICD-10 classification [BR:br08403]
 4. Endocrine, nutritional and metabolic diseases (E00-E90)
  E70-E90  Metabolic disorders
   E83  Disorders of mineral metabolism
    H01210  Hypomagnesemia
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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