Terminology Service for NFDI4Health

hereditary spastic paraplegia 55

Go to external page http://purl.obolibrary.org/obo/DOID_0110807


A hereditary spastic paraplegia that has_material_basis_in mutation in the C12ORF65 gene on chromosome 12q24. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 55

Synonyms
  • SPG55
  • autosomal recessive spastic paraplegia 55
  • autosomal recessive spastic paraplegia type 55
database cross reference
has obo namespace

disease_ontology

id

DOID:0110807