Terminology Service for NFDI4Health
JSON

hereditary spastic paraplegia 38

Go to external page http://purl.obolibrary.org/obo/DOID_0110789

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 4p16-p15. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 38

Synonyms
  • SPG38
  • autosomal dominant spastic paraplegia 38
  • autosomal dominant spastic paraplegia type 38
database cross reference
has obo namespace

disease_ontology

id

DOID:0110789