MeSH Browser

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: 128
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 MeSH Supplementary Concept Data 2024