hypomagnesemia 1, intestinal Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/602014
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1 genes associated with the hypomagnesemia 1, intestinal phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
TRPM6 transient receptor potential cation channel, subfamily M, member 6