Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline

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Subtype of: Neurodegeneration
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline
MONDO_0957985
CAPRIN1 Unknown
23849776 28135719 31398340 35977029 35979925 36136249
ClinGen, Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline.
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Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder 1 shared geneCAPRIN1 Related via 1 shared gene including CAPRIN1. Post-operative acute kidney injury 1 shared geneCAPRIN1 Related via 1 shared gene including CAPRIN1. Myoclonic epilepsy 1 shared geneCAPRIN1 Related via 1 shared gene including CAPRIN1. Moyamoya angiopathy 1 shared geneCAPRIN1 Related via 1 shared gene including CAPRIN1. Cerebellar ataxia 1 shared geneCAPRIN1 Related via 1 shared gene including CAPRIN1.