WormBase Tree Display for DO_term: DOID:0110812

DOID:0110812 Name: hereditary spastic paraplegia 61
  Status: Valid
  Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the ARL6IP1 gene on chromosome 16p12.
  Synonym: Exact: SPG61
      autosomal recessive spastic paraplegia 61
      autosomal recessive spastic paraplegia type 61
  Parent: Is_a: DOID:2476
      DOID:0050737
  DB_info: Database: OMIM disease 615685