Hypomyelination, global cerebral

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Hypomyelination, global cerebral
MONDO_0013056
SLC25A12 Unknown
27290639 19641205 27604308 24515575 25655951 31403263 26633542
Open Targets
All1 Causal0 Unknown1
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Epileptic encephalopathy, early infantile, 39 1 shared geneSLC25A12 Related via 1 shared gene including SLC25A12. Epileptic encephalopathy with global cerebral demyelination 1 shared geneSLC25A12 Related via 1 shared gene including SLC25A12. Delayed psychomotor development 1 shared geneSLC25A12 Related via 1 shared gene including SLC25A12. Asperger syndrome 1 shared geneSLC25A12 Related via 1 shared gene including SLC25A12. Developmental and epileptic encephalopathy 1 shared geneSLC25A12 Related via 1 shared gene including SLC25A12.