WormBase Tree Display for DO_term: DOID:0110799

DOID:0110799 Name: hereditary spastic paraplegia 47
  Status: Valid
  Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the AP4B1 gene on chromosome 1p13.
  Synonym: Exact: CPSQ5
      SPG47
      autosomal recessive spastic paraplegia 47
      spastic quadriplegic cerebral palsy 5
  Parent: Is_a: DOID:2476
      DOID:0050737
  DB_info: Database: OMIM disease 614066