Human genes for lissencephaly 10
Lissencephaly 10 [DOID:0112229]
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 CEP85L on chromosome 6q22.31.
Synonyms: lissencephaly 10, DOID:0112229, LIS10