WormMine: OntologyRelation

• Relationship: is_a
• Parent Term . Identifier: DOID:630
• Child Term . Identifier: DOID:0110333
• Direct: false
• Redundant: false

1 Child Term

• Identifier: DOID:0110333
• Name: Leber congenital amaurosis 7
• Description: A Leber congenital amaurosis that has_material_basis_in mutation in the CRX gene on chromosome 19q13.

1 Parent Term

• Identifier: DOID:630
• Name: genetic disease
• Description: A disease that has_material_basis_in genetic variations in the human genome.