Terminology Service for NFDI4Health

hereditary spastic paraplegia 75

Go to external page http://purl.obolibrary.org/obo/DOID_0110820


A hereditary spastic paraplegia that has_material_basis_in mutation in the MAG gene on chromosome 19q13. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 75

Synonyms
  • SPG75
  • autosomal recessive spastic paraplegia 75
  • autosomal recessive spastic paraplegia type 75
database cross reference
has obo namespace

disease_ontology

id

DOID:0110820