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GTR Home > Conditions/Phenotypes > Renal hypomagnesemia 2

Renal hypomagnesemia 2

Synonyms
Magnesium loss, isolated renal
Modes of inheritance
Autosomal dominant inheritance (Orphanet)

Summary

Autosomal dominant renal hypomagnesium wasting (HOMG2) is characterized by hypomagnesemia due to renal magnesium loss and is associated with hypocalciuria. Patients may have convulsions and muscle cramps, but they may also be asymptomatic except for the development of chondrocalcinosis at an adult age (summary by Knoers, 2009 and de Baaij et al., 2015). For a discussion of genetic heterogeneity of renal hypomagnesemia, see 602014. [from OMIM]

Available tests

31 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (31 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: ATP1G1, HOMG2, FXYD2
    Summary: FXYD domain containing ion transport regulator 2

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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