A comprehensive DNA test that screens 22 genes for inherited phosphate wasting, vitamin D metabolism defects, kidney tubular disorders, and bone mineralization conditions.


Phosphate wasting disorders
Genes that cause the kidneys to lose too much phosphate, leading to soft or bowed bones. PHEX is the most common cause of inherited rickets.
Vitamin D metabolism & response
Genes needed to activate or respond to vitamin D. Defects cause rickets that may or may not respond to standard vitamin D supplements.
Kidney tubular disorders
Genes behind kidney tubule disorders that leak phosphate along with other minerals. Rickets is one feature of broader kidney or metabolic conditions.
Bone mineralization defects
Genes that directly affect how minerals are deposited into bone. ALPL deficiency (hypophosphatasia) mimics rickets but has a different treatment approach.
Know your genetic risks. Share with your doctor. Build a stronger treatment plan.