neurodevelopmental disorder with cerebellar atrophy and with or without seizures

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Neurodevelopmental disorder with cerebellar atrophy and with or without seizures
BRAT1 Causal
39032489 26494257 26483087 27282546
ClinGen —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with neurodevelopmental disorder with cerebellar atrophy and with or without seizures.
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Lethal neonatal rigidity and multifocal seizure syndrome 1 shared geneBRAT1 Related via 1 shared gene including BRAT1. Rigidity and multifocal seizure syndrome, lethal neonatal 1 shared geneBRAT1 Related via 1 shared gene including BRAT1. neonatal-onset encephalopathy with rigidity and seizures 1 shared geneBRAT1 Related via 1 shared gene including BRAT1. Lethal congenital contracture syndrome 1 shared geneBRAT1 Related via 1 shared gene including BRAT1. Intellectual developmental disorder 1 shared geneBRAT1 Related via 1 shared gene including BRAT1.