WormMine: OntologyRelation

• Relationship: is_a
• Parent Term . Identifier: DOID:53
• Child Term . Identifier: DOID:0061020
• Direct: false
• Redundant: false

1 Child Term

• Identifier: DOID:0061020
• Name: combined pituitary hormone deficiency 2
• Description: A combined pituitary hormone deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the PROP1 gene on chromosome 5q35.

1 Parent Term

• Identifier: DOID:53
• Name: pituitary gland disease
• Description: An endocrine system disease that is located_in the pituitary gland.