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Cardiofaciocutaneous syndrome 2

MONDO:0014112

Any cardiofaciocutaneous syndrome in which the cause of the disease is a mutation in the KRAS gene.

Also known as: KRAS cardiofaciocutaneous syndrome, cardiofaciocutaneous syndrome 2, cardiofaciocutaneous syndrome caused by mutation in KRAS, cardiofaciocutaneous syndrome caused by mutation in kras, cardiofaciocutaneous syndrome type 2, kras cardiofaciocutaneous syndrome, CFC2

12 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) Cardiomyopathy (144) Skin disorder (132) Hypertrophic cardiomyopathy (112) Muscle tissue disorder (56) Syndromic disease (25)
Trials to join now! 9 Not yet recruiting 1 Not yet finished but already full! 2
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    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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