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Noonan syndrome 5

MONDO:0012690

Any Noonan syndrome in which the cause of the disease is a mutation in the RAF1 gene.

Also known as: NS5, Noonan syndrome 5, Noonan syndrome caused by mutation in RAF1, Noonan syndrome type 5, RAF1 Noonan syndrome, RAF1 gene related Noonan syndrome

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

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Broader categories

Cardiovascular disorder (1051) Disease (680) Heart disorder (300) Musculoskeletal system disorder (207) Hereditary disease (176) Immune system disorder (148) Cardiomyopathy (144) Lymphedema (139) Vascular disorder (135) Hypertrophic cardiomyopathy (112)
Trials to join now! 10 Not yet recruiting 1 Not yet finished but already full! 3
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  • Could you help scientists unlock genetic cancer secrets?

    Knowledge-focused Not yet recruiting

    This study screens up to 1,000 people with personal or family histories of certain cancers to see if they qualify for ongoing genetics research at the National Cancer Institute. Participants fill out a 15-20 minute online survey about their health and family history. No treatment…

    Sponsor: National Cancer Institute (NCI) • Aim: Knowledge-focused

    Last updated Aug 18, 2026 06:00 UTC

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