WormMine: OntologyRelation

• Relationship: is_a
• Parent Term . Identifier: DOID:2490
• Child Term . Identifier: DOID:0112235
• Direct: false
• Redundant: false

1 Child Term

• Identifier: DOID:0112235
• Name: lissencephaly 4
• Description: A microlissencephaly characterized by lissencephaly, severe brain atrophy, extreme microcephaly, and profound intellectual disability that has_material_basis_in homozygous or compound heterozygous mutation in the NDE1 gene on chromosome 16p13.11.

1 Parent Term

• Identifier: DOID:2490
• Name: congenital nervous system abnormality