lissencephaly 6 (DOID:0112236)
Alliance: disease page
Synonyms: LIS6
Alt IDs: OMIM:616212
Definition: A microlissencephaly characterized by severe microcephaly, developmental delay, lissencephaly, pachygyria, and hypoplasia of the corpus callosum that has_material_basis_in homozygous or compound heterozygous mutation in the KATNB1 gene on chromosome 16q21.