WormMine: OntologyRelation

• Relationship: is_a
• Parent Term . Identifier: DOID:2476
• Child Term . Identifier: DOID:0070458
• Direct: true
• Redundant: false

1 Child Term

• Identifier: DOID:0070458
• Name: hereditary spastic paraplegia 89
• Description: A hereditary spastic paraplegia characterized by infantile or early childhood onset of lower limb spasticity that has_material_basis_in homozygous mutation in the AMFR gene on chromosome 16q13.

1 Parent Term

• Identifier: DOID:2476
• Name: hereditary spastic paraplegia
• Description: A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs.