lissencephaly 10 (DOID:0112229)
Alliance: disease page
Synonyms: LIS10
Alt IDs: OMIM:618873
Definition: A lissencephaly characterized by variably delayed development, mildly to moderately impaired intellectual development and language delay, seizures, brain features consistent with neuronal migration defects that has_material_basis_in heterozygous mutation in the CEP85L gene on chromosome 6q22.31.