Terminology Service for NFDI4Health

hereditary spastic paraplegia 19

Go to external page http://purl.obolibrary.org/obo/DOID_0110772


A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 9q. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 19

Synonyms
  • SPG19
  • autosomal dominant spastic paraplegia 19
  • autosomal dominant spastic paraplegia type 19
database cross reference
has obo namespace

disease_ontology

id

DOID:0110772