Terminology Service for NFDI4Health

hereditary spastic paraplegia 77

Go to external page http://purl.obolibrary.org/obo/DOID_0110822


A hereditary spastic paraplegia that has_material_basis_in mutation in the FARS2 gene on chromosome 6p25. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 77

Synonyms
  • SPG77
  • autosomal recessive spastic paraplegia 77
database cross reference
has obo namespace

disease_ontology

id

DOID:0110822