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Telangiectasia, hereditary hemorrhagic, type 5

MONDO:0014217

Any hereditary hemorrhagic telangiectasia in which the cause of the disease is a mutation in the GDF2 gene.

Also known as: GDF2 hereditary hemorrhagic telangiectasia, GDF2 related HHT-like syndrome, hereditary hemorrhagic telangiectasia caused by mutation in GDF2, telangiectasia, hereditary hemorrhagic, type 5, HHT5

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

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Broader categories

Cardiovascular disorder (1051) Disease (680) Hereditary disease (176) Vascular disorder (135) Peripheral vascular disease (52) Hereditary hemorrhagic telangiectasia (31) Human disease (14) Telangiectasis (11) Developmental defect during embryogenesis (8) Capillary malformation (4)
Trials to join now! 3 Not yet finished but already full! 1
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  • New registry monitors VBX stent graft in Real-World use

    Knowledge-focused Ongoing

    This study is a registry that collects safety and performance data on the GORE® VIABAHN® VBX Stent Graft when used in peripheral vessels. It involves 280 adults who need this device to treat peripheral vascular disease. The goal is to see how well the stent graft works and if the…

    Sponsor: W.L.Gore & Associates • Aim: Knowledge-focused

    Last updated Jun 27, 2026 12:07 UTC

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