WormMine: OntologyRelation

• Relationship: is_a
• Parent Term . Identifier: DOID:225
• Child Term . Identifier: DOID:0080911
• Direct: false
• Redundant: false

1 Child Term

• Identifier: DOID:0080911
• Name: cerebrooculofacioskeletal syndrome 1
• Description: A cerebrooculofacioskeletal syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ERCC6 gene on chromosome 10q11.

1 Parent Term

• Identifier: DOID:225
• Name: syndrome
• Description: A disease characterized by a group of signs and symptoms that occur together and characterize a particular abnormality.