Myopathy, epilepsy, and progressive cerebral atrophy

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Subtype of: Cerebral atrophy · Myopathy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Myopathy, epilepsy, and progressive cerebral atrophy
MONDO_0033619
ALG14 Unknown
30221345 28733338 34971077 23404334 36200043
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Myopathy, epilepsy, and progressive cerebral atrophy.
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Intellectual developmental disorder seizures behavioral 1 shared geneALG14 Related via 1 shared gene including ALG14. Myasthenic syndrome, congenital, 15, without tubular aggregates 1 shared geneALG14 Related via 1 shared gene including ALG14. Intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies 1 shared geneALG14 Related via 1 shared gene including ALG14. Congenital myasthenic syndrome 1 shared geneALG14 Related via 1 shared gene including ALG14. Myasthenic syndrome 1 shared geneALG14 Related via 1 shared gene including ALG14.