# renal hypomagnesemia 3

> 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

**Wikidata**: [Q32136698](https://www.wikidata.org/wiki/Q32136698)  
**Source**: https://4ort.xyz/entity/renal-hypomagnesemia-3


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000113946/MONDO_0009550)
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)
6. UMLS 2023