Hereditary Hypophosphatemic Rickets With Hypercalciuria

About the Disease
Hypophosphatemic Rickets with Hypercalciuria, Hereditary, also known as hereditary hypophosphatemic rickets with hypercalciuria, is related to hypercalciuria, absorptive, 2 and bone disease, and has symptoms including muscle weakness, bone pain and difficulty standing. An important gene associated with Hypophosphatemic Rickets with Hypercalciuria, Hereditary is SLC34A3 (Solute Carrier Family 34 Member 3), and among its related pathways/superpathways are Disease and Diseases of glycosylation. Affiliated tissues include bone, cortex and kidney, and related phenotypes are hypercalciuria and increased circulating osteocalcin level

Common Targets
FGF23 | ENPP1 | SLC34A1 | SLC34A3 | DMP1

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