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 )

Relationships
is a type of: autosomal recessive disease lissencephaly