renal hypomagnesemia 3

MeSH: C537153ORPHA: 31043

Overview

hypomagnesemia characterized by autosomal recessive inheritance of excessive urinary Ca(2+) and Mg(2+) excretion that has material basis in homozygous or compound heterozygous mutation in the CLDN16 gene on chromosome 3q28

Available Treatments (0)

No treatments linked yet

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Classification & Codes

MeSH Code

C537153

Orphanet Code

ORPHA:31043
renal hypomagnesemia 3
MeSHC537153
OrphanetORPHA:31043
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO