WormBase Tree Display for DO_term: DOID:0110814

DOID:0110814 Name: hereditary spastic paraplegia 63
  Status: Valid
  Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the AMPD2 gene on chromosome 1p13.
  Synonym: Exact: SPG63
      autosomal recessive spastic paraplegia 63
      spastic paraplegia 63
  Parent: Is_a: DOID:2476
      DOID:0050737
  DB_info: Database: OMIM disease 615686
  Attribute_of: Gene_by_orthology: WBGene00016415