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Orofacial cleft 5

MONDO:0012142

Any orofacial cleft in which the cause of the disease is a mutation in the MSX1 gene.

Also known as: MSX1 orofacial cleft, orofacial cleft 5, orofacial cleft caused by mutation in MSX1, orofacial cleft type 5, OFC5, cleft lip with or without cleft palate, nonsyndromic, 5

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

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Broader categories

Disease (618) Musculoskeletal system disorder (196) Hereditary disease (172) Bone disorder (47) Cleft lip (24) Cleft lip/palate (24) Cleft lip and alveolus (15) Human disease (14) Disorder of facial skeleton (4) Orofacial cleft (4)
Trials to join now! 17 Not yet recruiting 6 Not yet finished but already full! 4 Completed 8 Terminated 1
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  • Scientists gather leftover surgical tissue to unlock secrets of bone disease

    Knowledge-focused Terminated

    This study collected bone, cartilage, skin, and fat tissue from 50 patients undergoing surgery at Children's National Medical Center. The goal was to grow cells from these tissues in the lab and analyze them to better understand bone and connective tissue diseases. The study was …

    Sponsor: National Institute of Dental and Craniofacial Research (NIDCR) • Aim: Knowledge-focused

    Last updated Jun 27, 2026 07:52 UTC

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