WormMine: OntologyRelation

• Relationship: is_a
• Parent Term . Identifier: DOID:7
• Child Term . Identifier: DOID:0111314
• Direct: false
• Redundant: false

1 Child Term

• Identifier: DOID:0111314
• Name: idiopathic generalized epilepsy 13
• Description: An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the GABRA1 on chromosome 5q34.

1 Parent Term

• Identifier: DOID:7
• Name: disease of anatomical entity
• Description: A disease that manifests in a defined anatomical structure.