Gene List:
ALPL, CLCN5, CYP27B1, CYP2R1, DMP1, ENPP1, FAH, FAM20C, FGF23, FGFR1, KL, PHEX, SLC34A1, SLC34A3, VDR

References:
Lin X, et al. Genetic analysis of three families with X-linked dominant hypophosphatemic rickets. Journal of Pediatric Endocrinology and Metabolism. 2018;31(7).

Bai Y, et al. Mutation analysis of four pedigrees affected with hypophosphatemic rickets through targeted next-generation sequencing. Chinese Journal of Medical Genetics. 2018 Oct;35(5):638-643.

Lal D, et al. Increased Probability of Co-Occurrence of Two Rare Diseases in Consanguineous Families and Resolution of a Complex Phenotype by Next Generation Sequencing. Plos One. 2016;11(1):e0146040.