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Striatal degeneration, autosomal dominant 2

Summary

Autosomal dominant striatal degeneration-2 is a neurologic disorder characterized by hyperkinetic movements, mainly chorea, resulting from dysfunction of the basal ganglia. Although symptoms appear in the first decade, the disorder is not progressive (summary by Mencacci et al., 2016). For a discussion of genetic heterogeneity of ADSD, see ADSD1 (609161). [from OMIM]

Available tests

9 tests are in the database for this condition.

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Clinical tests (9 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: ADSD2, HSPDE10A, IOLOD, LINC00473, PDE10A19, PDE10A
    Summary: phosphodiesterase 10A

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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