Neurodegeneration, infantile-onset, with optic atrophy and brain abnormalities

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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, infantile-onset, with optic atrophy and brain abnormalities
MONDO_0975837
BORCS8 Unknown
38128568
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Neurodegeneration, infantile-onset, with optic atrophy and brain abnormalities.
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Early-infantile neurological disorder with severe intellectual disability, hypotonia and congenital heart disease 1 shared geneBORCS8 Related via 1 shared gene including BORCS8. Genetic neurodegenerative disease 1 shared geneBORCS8 Related via 1 shared gene including BORCS8. Neurodevelopmental disorder 1 shared geneBORCS8 Related via 1 shared gene including BORCS8.