WormMine: OntologyRelation

• Relationship: is_a
• Parent Term . Identifier: DOID:936
• Child Term . Identifier: DOID:0050978
• Direct: false
• Redundant: false

1 Child Term

• Identifier: DOID:0050978
• Name: spinocerebellar ataxia type 29
• Description: An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, intellectual disability, dysarthria and ophthalmoplegia, and has_material_basis_in mutation in the ITPR1 gene.

1 Parent Term

• Identifier: DOID:936
• Name: brain disease
• Description: A central nervous system disease that is located_in the brain.