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GTR Home > Conditions/Phenotypes > Autosomal recessive spinocerebellar ataxia 15

Autosomal recessive spinocerebellar ataxia 15

Synonyms
SALIH ATAXIA
Modes of inheritance
Autosomal recessive inheritance (Orphanet)

Summary

Autosomal recessive spinocerebellar ataxia-15 (SCAR15) is characterized by early-onset ataxia, cognitive impairment, dysarthria, and developmental delay. Variable features include seizures, nystagmus, and abnormal reflexes (Seidahmed et al., 2020). [from OMIM]

Available tests

10 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (10 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: KIAA0226, RUBICON, SCAR15, RUBCN
    Summary: rubicon autophagy regulator

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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