Term Name:	Norman-Roberts syndrome
Synonyms:	lissencephaly 2, lissencephaly syndrome, Norman-Roberts type
Definition:	A lissencephaly that has_material_basis_in homozygous mutation in the gene encoding reelin (RELN) on chromosome 7q22.
Ontology:	Human Disease [DOID:0060902]   ( DOID:0060902 )