OBO ID: DOID:0110809
Term Name: hereditary spastic paraplegia 57 Search Ontology:
Synonyms:
  • autosomal recessive spastic paraplegia 57
  • autosomal recessive spastic paraplegia type 57
  • SPG57
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the TFG gene on chromosome 3q12. https://www.ncbi.nlm.nih.gov/pubmed/23479643
References:
Ontology: Human Disease   (DOID:0110809)
OTHER hereditary spastic paraplegia 57 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TFG ?Spastic paraplegia 57, autosomal recessive 615658
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None