Focal epilepsy-intellectual disability-cerebro-cerebellar malformation

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
FOCAL EPILEPSY, INTELLECTUAL DISABILITY, CEREBRO-CEREBELLAR MALFORMATION SYNDROME
C4707306
TBC1D24 Unknown — Disgenet
FOCAL EPILEPSY-INTELLECTUAL DISABILITY-CEREBRO-CEREBELLAR MALFORMATION
352587MONDO:0018125
TBC1D24 Unknown
23517570
Orphanet
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Focal epilepsy-intellectual disability-cerebro-cerebellar malformation.
5 View disease cluster →
Deafness, onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome 1 shared geneTBC1D24 Related via 1 shared gene including TBC1D24. Deafness with congenital onychodystrophy 1 shared geneTBC1D24 Related via 1 shared gene including TBC1D24. Doors syndrome 1 shared geneTBC1D24 Related via 1 shared gene including TBC1D24. Infantile myoclonic epilepsy 1 shared geneTBC1D24 Related via 1 shared gene including TBC1D24. Periodic paralysis 1 shared geneTBC1D24 Related via 1 shared gene including TBC1D24.