WormMine: OntologyRelation

• Relationship: is_a
• Parent Term . Identifier: DOID:0050177
• Child Term . Identifier: DOID:0110383
• Direct: false
• Redundant: false

1 Child Term

• Identifier: DOID:0110383
• Name: retinitis pigmentosa 7
• Description: A retinitis pigmentosa that has_material_basis_in mutation in the PRPH2 gene on chromosome 6p21.

1 Parent Term

• Identifier: DOID:0050177
• Name: monogenic disease
• Description: A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive.