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.

Noonan Syndrome

Prevalence: 1/2500

cardiac

Official·OMIM:163950 Official·ORPHA648

Short stature and congenital heart disease due to PTPN11 and other RAS/MAPK pathway gene mutations.

Associated Genes

No gene records found associated with this disease.