Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity

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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 and structural brain anomalies with or without seizures and spasticity
MONDO_0030046
PTPN23 Causal
29899372 25558065 29090338 27848944 31395947
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity.
5 View disease cluster →
Neurodevelopmental disorder with or without structural brain anomalies, optic atrophy, seizures and spasticity 1 shared genePTPN23 Related via 1 shared gene including PTPN23. Brain atrophy 1 shared genePTPN23 Related via 1 shared gene including PTPN23. Hereditary spastic paraplegia 1 shared genePTPN23 Related via 1 shared gene including PTPN23. Non-specific syndromic intellectual disability 1 shared genePTPN23 Related via 1 shared gene including PTPN23. Intellectual disability 1 shared genePTPN23 Related via 1 shared gene including PTPN23.