Other Names for this Disease
- Hypomagnesemia, familial, with hypercalciuria and nephrocalcinosis
- Hypomagnesemia, isolated renal
- Magnesium, defect in renal tubular transport of
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- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Hypomagnesemia primary. Click on the link to view a sample search on this topic.