| Disease Aliases (20) | Familial primary hypomagnesemia with hypocalcuria Homg Homg1 Hsh Hypomagnesemia with secondary hypocalcemia Hypomagnesemia, intestinal, with secondary hypocalcemia Hypomagnesemic tetany Hypomagnesemia caused by selective magnesium malabsorption Hypomagnesemia intestinal type 1 Intestinal hypomagnesemia with secondary hypocalcemia Phsh Primary hypomagnesemia with secondary hypocalcemia Trpm6 familial primary hypomagnesemia Trpm6 primary hypomagnesemia Familial primary hypomagnesemia caused by mutation in trpm6 Hypomagnesemia 1, intestinal Hypomagnesemia 1, intestinal; homg1 Intestinal hypomagnesemia type 1 Primary hypomagnesemia caused by mutation in trpm6 |
Associated Genes (1) NCBI-RefSeq: TRPM6 (Transient receptor potential cation channel subfamily M member 6) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Intestinal hypomagnesemia 1 | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |