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Spondylocostal dysostosis 5

MONDO:0007389

Any spondylocostal dysostosis in which the cause of the disease is a mutation in the TBX6 gene.

Also known as: SCDO5, TBX6 spondylocostal dysostosis, costovertebral segmentation anomalies, scoliosis, congenital, with or without rib anomalies, spondylocostal dysostosis 5, spondylocostal dysostosis caused by mutation in TBX6, spondylocostal dysostosis type 5, spondylothoracic dysostosis

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

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Broader categories

Disease (618) Musculoskeletal system disorder (196) Hereditary disease (172) Vertebral column disorder (74) Bone disorder (47) Human disease (14) Spondylocostal dysostosis (5) Skeletal system disorder (4) Bone development disease (2) Disease of genetic or genomic mechanism (2)
Trials to join now! 25 Not yet recruiting 8 Not yet finished but already full! 6 Completed 16 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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