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Spastic ataxia 1

MONDO:0007164

Any autosomal dominant spastic ataxia in which the cause of the disease is a mutation in the VAMP1 gene.

Also known as: SPAX1, VAMP1 autosomal dominant spastic ataxia, autosomal dominant spastic ataxia caused by mutation in VAMP1, spastic ataxia type 1, autosomal dominant spastic ataxia type 1, spastic ataxia 1, autosomal dominant

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

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Broader categories

Disease (717) Nervous system disorder (243) Hereditary disease (188) Human disease (15) Hereditary neurological disease (6) Atactic disorder (5) Disease of genetic or genomic mechanism (2) Hereditary ataxia (2) Spastic ataxia (1) Autosomal dominant disease (0)
Trials to join now! 1
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  • Can a massive natural history study unlock the secrets of rare movement disorders?

    Knowledge-focused Recruiting now

    This study follows thousands of people with ataxia, hereditary spastic paraplegia, and spastic ataxia, rare conditions that cause progressive problems with walking, balance, and coordination. Researchers will track how symptoms evolve using clinical exams, patient reports, digita…

    Sponsor: Heidelberg University • Aim: Knowledge-focused

    Last updated Sep 03, 2026 00:00 UTC

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