Terminology Service for NFDI4Health

hereditary spastic paraplegia 51

Go to external page http://purl.obolibrary.org/obo/DOID_0110803


A hereditary spastic paraplegia that has_material_basis_in mutation in the AP4E1 gene on chromosome 15q21. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 51

Synonyms
  • CPSQ4
  • SPG51
  • autosomal dominant spastic paraplegia 51
  • spastic quadriplegic cerebral palsy 4
database cross reference
has obo namespace

disease_ontology

id

DOID:0110803