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Tremor, hereditary essential, 1

MONDO:0008590

Any essential tremor in which the cause of the disease is a mutation in the DRD3 gene.

Also known as: DRD3 essential tremor, essential tremor caused by mutation in DRD3, essential tremor, hereditary, 1, tremor, hereditary essential, 1, tremor, hereditary essential, type 1, ETM1, FET1, tremor familial essential, 1

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

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Movement disorder (89) Essential tremor (85) Human disease (14) Hereditary neurological disease (5) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0)
Trials to join now! 10 Not yet recruiting 1 Completed 2
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  • New study aims to uncover hidden clot risks after major aortic surgery

    Knowledge-focused Not yet recruiting

    This study will look at 800 patients who had aortic surgery to understand why some develop dangerous blood clots inside the repaired artery. Researchers want to find out how common these clots are, what puts patients at risk, and how they affect recovery. The goal is to improve c…

    Sponsor: Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico • Aim: Knowledge-focused

    Last updated Jun 27, 2026 12:00 UTC

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