The information on this page is for informational purposes only and does not constitute medical advice. Consult your genetic counselor or specialist physician for treatment decisions.

Congenital Central Hypoventilation Syndrome

Prevalence: 1/200000
respiratory
Official·OMIM:209880Official·ORPHA661

Autonomic breathing control disorder due to PHOX2B gene mutations.

Associated Genes

No gene records found associated with this disease.