Terminology Service for NFDI4Health

hereditary spastic paraplegia 29

Go to external page http://purl.obolibrary.org/obo/DOID_0110780


A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1p31.1-p21.1. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 29

Synonyms
  • SPG29
  • autosomal dominant spastic paraplegia 29
database cross reference
has obo namespace

disease_ontology

id

DOID:0110780