National Center for Advancing and Translational Sciences Genetic and Rare Diseases Information Center, a program of the National Center for Advancing and Translational Sciences

Hypophosphatemic rickets



I was diagnosed with hypophosphatemic rickets 24 years ago. My brother is not affected. Are my future children at risk to have this condition?


Because I have hypophosphatemic rickets, are my children at risk to have the same condition?

Hypophosphatemic rickets is a genetic condition. This puts your children at risk to inherit the gene mutation that causes the disease. The chance that your child would inherit the condition depends on the inheritance pattern in your family. Hypophosphatemic rickets is most commonly inherited in an X-linked dominant pattern, but some families have been found to have an X-linked recessive, autosomal dominant and autosomal recessive inheritance patterns.[1] To learn about which inheritance pattern is in your family and the specific risks to your future children, we recommend that you consult with a genetics professional.
Last updated: 7/2/2018

How can I find a genetics professional in my area?

To find a medical professional who specializes in genetics, you can ask your doctor for a referral or you can search for one yourself. Online directories are provided by the American College of Medical Genetics and the National Society of Genetic Counselors. If you need additional help, contact a GARD Information Specialist. You can also learn more about genetic consultations from Genetics Home Reference.
Last updated: 12/6/2017

We hope this information is helpful. We strongly recommend you discuss this information with your doctor. If you still have questions, please contact us.

Warm regards,
GARD Information Specialist

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  1. Hereditary hypophosphatemic rickets. Genetics Home Reference. September 2010; http://ghr.nlm.nih.gov/condition/hereditary-hypophosphatemic-rickets. Accessed 12/13/2016.