neurodegeneration, childhood-onset, with cerebellar atrophy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
neurodegeneration, childhood-onset, with cerebellar atrophy
AGTPBP1 Causal
28600779 30420557 30976113 31102495
ClinGen —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with neurodegeneration, childhood-onset, with cerebellar atrophy.
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Congenital pontocerebellar hypoplasia 1 shared geneAGTPBP1 Related via 1 shared gene including AGTPBP1. Cerebellar atrophy 1 shared geneAGTPBP1 Related via 1 shared gene including AGTPBP1. Pontocerebellar hypoplasia 1 shared geneAGTPBP1 Related via 1 shared gene including AGTPBP1. Global developmental delay 1 shared geneAGTPBP1 Related via 1 shared gene including AGTPBP1. Neurodevelopmental disorder 1 shared geneAGTPBP1 Related via 1 shared gene including AGTPBP1.