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Hypomagnesemia primary MeSH Supplementary Concept Data 2022


MeSH Supplementary
Hypomagnesemia primary
Unique ID
C537153
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C537153
Entry Term(s)
Hypomagnesemia 3, Renal
Hypomagnesemia, Primary, Due To Defect In Renal Tubular Transport Of Magnesium
Hypomagnesemia, familial, with hypercalciuria and nephrocalcinosis
Hypomagnesemia, isolated renal
Magnesium, defect in renal tubular transport of
Registry Number
0
Heading Mapped to
*Nephrocalcinosis
*Renal Tubular Transport, Inborn Errors
*Hypercalciuria
Frequency
127
Note
A progressive renal disorder characterized by excessive urinary Ca(2+) and Mg(2+) excretion. There is progressive loss of kidney function, and in about 50% of cases, the need for renal replacement therapy by the second decade of life. Germline mutations in the CLDN16 gene have been identified. OMIM: 603959
Date of Entry
2010/08/25
Revision Date
2015/08/18
Hypomagnesemia primary Preferred
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