OBO ID: DOID:0110822
Term Name: hereditary spastic paraplegia 77 Search Ontology:
Synonyms:
  • autosomal recessive spastic paraplegia 77
  • SPG77
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the FARS2 gene on chromosome 6p25. https://www.ncbi.nlm.nih.gov/pubmed/26553276
References:
Ontology: Human Disease   (DOID:0110822)
OTHER hereditary spastic paraplegia 77 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FARS2 Spastic paraplegia 77, autosomal recessive 617046
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None