Terminology Service for NFDI4Health

hereditary spastic paraplegia 53

Go to external page http://purl.obolibrary.org/obo/DOID_0110805


A hereditary spastic paraplegia that has_material_basis_in mutation in the VPS37A gene on chromosome 8p22. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 53

Synonyms
  • SPG53
  • autosomal recessive spastic paraplegia 53
  • autosomal recessive spastic paraplegia type 53
database cross reference
has obo namespace

disease_ontology

id

DOID:0110805