# renal hypomagnesemia 2

> hypomagnesemia characterized by autosomal dominant inheritance of hypomagnesemia due to renal magnesium loss that has material basis in heterozygous mutation in the FXYD2 gene on chromosome 11q23

**Wikidata**: [Q32136745](https://www.wikidata.org/wiki/Q32136745)  
**Source**: https://4ort.xyz/entity/renal-hypomagnesemia-2


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. Human Phenotype Ontology release 2018-03-08
4. UniProt
5. Dominant isolated renal magnesium loss is caused by misrouting of the Na(+),K(+)-ATPase gamma-subunit
6. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)