Subtype of: Microcephaly, seizures, and developmental delay · Pachygyria

Pathways column key: KEGG Reactome

Disease Term	Disease ID	Gene Symbol	Classification	References	Source	Pathways
Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures	MONDO_0032893	TUBGCP2	Causal	31630790 40017707	Open Targets	Recruitment of mitotic centrosome proteins and complexes Recruitment of NuMA to mitotic centrosomes

Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures