Microcephaly 2, Primary, Autosomal Recessive, with or Without Cortical Malformations (MCPH2)

Microcephaly 2, Primary, Autosomal Recessive, with or Without Cortical Malformations, also known as mcph2, is related to primary microcephaly and microcephaly 5, primary, autosomal recessive, and has symptoms including hemiparesis An important gene associated with Microcephaly 2, Primary, Autosomal Recessive, with or Without Cortical Malformations is WDR62 (WD Repeat Domain 62), and among its related pathways/superpathways is Complement cascade. Affiliated tissues include brain and cerebellum, and related phenotypes are intellectual disability and global developmental delay