WormMine: OntologyRelation

• Relationship: is_a
• Parent Term . Identifier: DOID:7
• Child Term . Identifier: DOID:0111022
• Direct: false
• Redundant: false

1 Child Term

• Identifier: DOID:0111022
• Name: cone-rod dystrophy 16
• Description: A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the C8ORF37 gene on chromosome 8q22.

1 Parent Term

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