Primary microcephaly, cortical malformation, and epileptic encephalopathy

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Subtype of: Primary microcephaly
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
primary microcephaly, cortical malformation, and epileptic encephalopathy
MONDO_0032887
TMX2 Unknown
31735293
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Primary microcephaly, cortical malformation, and epileptic encephalopathy.
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Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity 1 shared geneTMX2 Related via 1 shared gene including TMX2. Congenital neurologic anomalies 1 shared geneTMX2 Related via 1 shared gene including TMX2. Anxiety disorder 1 shared geneTMX2 Related via 1 shared gene including TMX2. Neurodevelopmental disorder 1 shared geneTMX2 Related via 1 shared gene including TMX2. Autism 1 shared geneTMX2 Related via 1 shared gene including TMX2.