Miller-Dieker Lissencephaly Syndrome, also known as miller-dieker syndrome, is related to pachygyria and polymicrogyria, and has symptoms including seizures An important gene associated with Miller-Dieker Lissencephaly Syndrome is PAFAH1B1 (Platelet Activating Factor Acetylhydrolase 1b Regulatory Subunit 1), and among its related pathways/superpathways are Cell Cycle, Mitotic and Vesicle-mediated transport. Affiliated tissues include brain and kidney, and related phenotypes are intellectual disability and motor delay