nephrolithiasis/osteoporosis, hypophosphatemic, 2 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/612287
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Genes

1 genes associated with the nephrolithiasis/osteoporosis, hypophosphatemic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SLC9A3R1 solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1