01
ATP12A
ATPase H+/K+ transporting non-gastric alpha2 subunit
ATPase H+/K+ transporting non-gastric alpha2 subunit
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 6
Basic Information
Grouped by core information, identifiers, and descriptions.
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Core Information
- Disease Name
- Magnesium Deficiency
- Standard Disease Name
- magnesium deficiency
- MeSH Tree
- No data
- ICD-10
- E61.2
Identifiers
- DO ID
- No data
- MeSH ID
- D008275
- OMIM ID
- No data
- UMLS ID
- C0024473
- HPO ID
- No data
Description and Extensions
- Description
- MSH2017_2016_08_12:A nutritional condition produced by a deficiency of magnesium in the diet, characterized by anorexia, nausea, vomiting, lethargy, and weakness. Symptoms are paresthesias, muscle cramps, irritability, decreased attention span, and mental confusion, possibly requiring months to appear. Deficiency of body magnesium can exist even when serum values are normal. In addition, magnesium deficiency may be organ-selective, since certain tissues become deficient before others. (Harrison's Principles of Internal Medicine, 12th ed, p1936)|CSP2006:condition due to decreased dietary intake of magnesium, as in starvation or failure to administer in intravenous solutions, or to gastrointestinal loss; deficiency causes irritability of the nervous system with tetany, vasodilation, convulsions, tremors, depression, and psychotic behavior.
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Related Targets
target disease6 Targets