Terminology Service for NFDI4Health

hereditary spastic paraplegia 52

Go to external page http://purl.obolibrary.org/obo/DOID_0110804


A hereditary spastic paraplegia that has_material_basis_in mutation in the AP4S1 gene on chromosome 14q12. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 52

Synonyms
  • CPSQ6
  • SPG52
  • autosomal recessive spastic paraplegia 52
  • spastic quadriplegic cerebral palsy 6
database cross reference
has obo namespace

disease_ontology

id

DOID:0110804