Autosomal recessive cerebellar ataxia

Log in to bookmark this disease

Bookmark This Disease

Subtype of: Cerebellar ataxia
Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • autosomal recessive cerebellar ataxia
MONDO_0014503
CWF19L1 Unknown
15981765 25361784 26197978 27016154 30167849
ClinGen, Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Autosomal recessive cerebellar ataxia.
5 View disease cluster →
Developmental delay with epilepsy, progressive ataxia and cerebellar atrophy 1 shared geneCWF19L1 Related via 1 shared gene including CWF19L1. Spinocerebellar ataxia 1 shared geneCWF19L1 Related via 1 shared gene including CWF19L1. Cerebellar ataxia 1 shared geneCWF19L1 Related via 1 shared gene including CWF19L1. Upper aerodigestive tract neoplasm 1 shared geneCWF19L1 Related via 1 shared gene including CWF19L1. Nonalcoholic fatty liver disease 1 shared geneCWF19L1 Related via 1 shared gene including CWF19L1.