Search Ontology:
Human Disease

hereditary spastic paraplegia 77

Term ID
DOID:0110822
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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