WormMine: OntologyRelation

• Relationship: is_a
• Parent Term . Identifier: DOID:936
• Child Term . Identifier: DOID:0111313
• Direct: false
• Redundant: false

1 Child Term

• Identifier: DOID:0111313
• Name: idiopathic generalized epilepsy 12
• Description: An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the SLC2A1 on chromosome 1p34.2.

1 Parent Term

• Identifier: DOID:936
• Name: brain disease
• Description: A central nervous system disease that is located_in the brain.