Developmental delay with epilepsy, progressive ataxia and cerebellar atrophy

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Subtype of: Cerebellar ataxia · Developmental delay
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • developmental delay with epilepsy, progressive ataxia and cerebellar atrophy
MONDO_0014503
CWF19L1 Unknown
25361784 26197978 27016154 33012273 36453471
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Developmental delay with epilepsy, progressive ataxia and cerebellar atrophy.
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Autosomal recessive cerebellar ataxia 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.