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Cornelia de Lange syndrome 4

MONDO:0013864

Any Cornelia de Lange syndrome in which the cause of the disease is a mutation in the RAD21 gene.

Also known as: Cornelia De Lange syndrome type 4, Cornelia de Lange syndrome 4, Cornelia de Lange syndrome caused by mutation in RAD21, RAD21 Cornelia de Lange syndrome, CDLS4, Cornelia DE Lange syndrome 4

1 clinical trial for this condition and its sub-types.

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Broader categories

Disease (680) Musculoskeletal system disorder (207) Hereditary disease (176) Bone disorder (51) Syndromic disease (25) Human disease (14) Developmental defect during embryogenesis (8) Cornelia de Lange syndrome (4) Skeletal system disorder (4) Congenital limb malformation (3)
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  • Kids test new bionic foot design

    Knowledge-focused Completed

    This study tested a new prosthetic foot for children with leg amputations or birth defects. Thirteen kids walked with the device and gave feedback on stiffness and performance. The goal was to gather ideas to improve future foot designs.

    Sponsor: Össur Iceland ehf • Aim: Knowledge-focused

    Last updated Jun 27, 2026 14:00 UTC

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