Microcephaly, Autosomal Dominant, also known as microcephaly autosomal dominant, is related to microcephaly 18, primary, autosomal dominant and microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development. An important gene associated with Microcephaly, Autosomal Dominant is KIF11 (Kinesin Family Member 11), and among its related pathways/superpathways are EML4 and NUDC in mitotic spindle formation and 15q11.2 copy number variation syndrome. Affiliated tissues include brain, and related phenotypes are Mitotic arrest, spindle defect and nervous system