WormBase Tree Display for DO_term: DOID:0110773

DOID:0110773 Name: hereditary spastic paraplegia 2
  Status: Valid
  Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the PLP1 gene on chromosome Xq22.2.
  Synonym: Exact: SPG2
      X-linked spastic paraplegia 2
      spastic paraplegia type 2
  Parent: Is_a: DOID:2476
      DOID:0080012
  DB_info: Database: OMIM disease 312920
  Attribute_of: Gene_by_orthology: WBGene00017437