Neurodevelopmental disorder with epilepsy and brain atrophy

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Subtype of: Neurodevelopmental disorder
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Neurodevelopmental disorder with epilepsy and brain atrophy
MONDO_0859265
ATP6V0A1 Causal
33833240 34909687
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder with epilepsy and brain atrophy.
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Esophageal atresia 1 shared geneATP6V0A1 Related via 1 shared gene including ATP6V0A1. Developmental disorder 1 shared geneATP6V0A1 Related via 1 shared gene including ATP6V0A1. Cerebellar ataxia 1 shared geneATP6V0A1 Related via 1 shared gene including ATP6V0A1. Seizures 1 shared geneATP6V0A1 Related via 1 shared gene including ATP6V0A1. Developmental and epileptic encephalopathy 1 shared geneATP6V0A1 Related via 1 shared gene including ATP6V0A1.