WormMine: OntologyRelation

• Relationship: is_a
• Parent Term . Identifier: DOID:7
• Child Term . Identifier: DOID:6620
• Direct: false
• Redundant: false

1 Child Term

• Identifier: DOID:6620
• Name: X-linked hyper IgM syndrome
• Description: A hyper IgM syndrome that is characterized by neutropenia and a high rate of gastrointestinal and central nervous system infections and that has_material_basis_in a mutation in the CD40LG gene on chromosome Xq26.3.

1 Parent Term

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