Terminology Service for NFDI4Health

hereditary spastic paraplegia 45

Go to external page http://purl.obolibrary.org/obo/DOID_0110797


A hereditary spastic paraplegia that has_material_basis_in mutation in the NT5C2 gene on chromosome 10q24. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 45

Synonyms
  • SPG45
  • SPG65
  • autosomal recessive spastic paraplegia 45
  • autosomal recessive spastic paraplegia type 45
  • autosomal recessive spastic paraplegia type 65
database cross reference
has obo namespace

disease_ontology

id

DOID:0110797