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QuickView for cerebellar ataxia (phenotype)


Genetic Markers

Most Correlated Genes

Most Correlated SNPs

  1. ATXN3
  2. APTX
  3. KCNA1
  4. RORA
  5. EXOSC5
  1. No SNPs found
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Pathway Enrichment

Most Correlated Biogroups

  1. Voltage-dependent channel domain superfamily
  2. Ion transport domain
  3. cellular potassium ion transport
  4. potassium ion transmembrane transport
  5. transmission of nerve impulse
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Curated Studies

Most Correlated Studies

  1. Mouse Phenotypes - Autosomal dominant hereditary disorder
  2. OMIM - Cerebellar ataxia
  3. OMIM - CAPOS syndrome
  4. OMIM - Ataxia
  5. Epithelial cells from kidney organoids of Mainzer-Saldino syndrome patient iPSC with IFT140 mutation
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Literature

Most Relevant Literature

  1. Consensus Paper: Latent Autoimmune Cerebellar Ataxia (LACA).
  2. Gene Suppression Therapies in Hereditary Cerebellar Ataxias: A Systematic Review of Animal Studies.
  3. Neuronal antibodies in nonparaneoplastic autoimmune cerebellar ataxias.
  4. Recent advances in diagnosis of immune-mediated cerebellar ataxias: novel concepts and fundamental q…
  5. Immune-Mediated Cerebellar Ataxias].
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Clinical Trials

Most Relevant Clinical Trials

  1. A Registered Cohort Study on Cerebellar Ataxia
  2. Augmenting Balance in Individuals With Cerebellar Ataxias
  3. Effect of Riluzole as a Symptomatic Approach in Patients With Chronic Cerebellar Ataxia
  4. Efficacy of Riluzole in Hereditary Cerebellar Ataxia
  5. Dual Task Training for Cerebellar Ataxia
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