Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity

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Subtype of: Neurodevelopmental disorder
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity
MONDO_0032887
TMX2 Causal
31735293 31586943 31270415
Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity.
5 View disease cluster →
Primary microcephaly, cortical malformation, and epileptic encephalopathy 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.