WormMine: OntologyRelation

• Relationship: is_a
• Parent Term . Identifier: DOID:0050739
• Child Term . Identifier: DOID:0110795
• Direct: false
• Redundant: false

1 Child Term

• Identifier: DOID:0110795
• Name: hereditary spastic paraplegia 43
• Description: A hereditary spastic paraplegia that has_material_basis_in mutation in the C19ORF12 gene on chromosome 19q12.

1 Parent Term

• Identifier: DOID:0050739
• Name: autosomal genetic disease
• Description: A monogenic disease that has_material_basis_in a mutation in a single gene on one of the non-sex chromosomes.