Term Name: lissencephaly 10
Synonyms: LIS10
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.
Ontology: Human Disease [DOID:0112229]   ( DOID:0112229 )

Relationships
is a type of: autosomal dominant disease lissencephaly