Term Name:	X-linked lissencephaly 1
Synonyms:	lissencephaly type 1 due to doublecortin gene mutation, XLIS1
Definition:	A lissencephaly characterized by classic lissencephaly and intellectual disability in males that has_material_basis_in mutation in DCX on chromosome Xq23.
Ontology:	Human Disease [DOID:0112239]   ( DOID:0112239 )