Noonan syndrome 8

MONDO:0014143

Any Noonan syndrome in which the cause of the disease is a mutation in the RIT1 gene.

Also known as: NS8, Noonan syndrome 8, Noonan syndrome caused by mutation in RIT1, Noonan syndrome type 8, RIT1 Noonan syndrome

241 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by