Encephalopathy, neonatal severe

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Subtype of: Encephalopathy · Neonatal encephalopathy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Encephalopathy neonatal severe due to MECP2 mutations
MONDO_0010397
MECP2 Unknown
10232754 10508514 10577905 10767337 10814718 10854091 11007980 11022934 11214906 11238684 11313756 11402105 11807877 11930274 12161600 12481990 12615169 15034579 15689435 15857422 16630165 16966553 18989701 19034540 29618507 9377804
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Encephalopathy, neonatal severe.
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Central apnea 1 shared geneMECP2 Related via 1 shared gene including MECP2. Neonatal encephalopathy 1 shared geneMECP2 Related via 1 shared gene including MECP2. Bruxism 1 shared geneMECP2 Related via 1 shared gene including MECP2. Bulbar palsy 1 shared geneMECP2 Related via 1 shared gene including MECP2. Chromosome xq28 duplication syndrome 1 shared geneMECP2 Related via 1 shared gene including MECP2.