Terminology Service for NFDI4Health
JSON

hereditary spastic paraplegia 46

Go to external page http://purl.obolibrary.org/obo/DOID_0110798

A hereditary spastic paraplegia that has_material_basis_in mutation in the GBA2 gene on chromosome 9p. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 46

Synonyms
  • SPG46
  • autosomal recessive spastic paraplegia 46
  • autosomal recessive spastic paraplegia type 46
database cross reference
has obo namespace

disease_ontology

id

DOID:0110798