WormBase Tree Display for DO_term: DOID:0110801

DOID:0110801 Name: hereditary spastic paraplegia 49
  Status: Valid
  Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the TECPR2 gene on chromosome 14q32.
  Synonym: Exact: SPG49
      autosomal recessive spastic paraplegia 49
      autosomal recessive spastic paraplegia type 49
  Parent: Is_a: DOID:2476
      DOID:0050737
  DB_info: Database: OMIM disease 615031