spinocerebellar ataxia, autosomal recessive 29

Rare Disease

MONDO:0030312

Also known as:

Barakat-Van Ham-Kaya syndromeSCAR29neurodevelopmental disorder with hypotonia and cerebellar ataxia

Genes

Clinical Trials

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Newborn Screening

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Patient Groups

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Companies Active in spinocerebellar ataxia, autosomal recessive 29

1 company

Organizations with orphan designations or approved therapies for this disease

Atamyo Therapeutics

Other

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