Terminology Service for NFDI4Health

hereditary spastic paraplegia 72

Go to external page http://purl.obolibrary.org/obo/DOID_0110817


A hereditary spastic paraplegia that has_material_basis_in mutation in the REEP2 gene on chromosome 5q31. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 72

Synonyms
  • SPG72
  • autosomal spastic paraplegia type 72
database cross reference
has obo namespace

disease_ontology

id

DOID:0110817