Terminology Service for NFDI4Health

hereditary spastic paraplegia 30

Go to external page http://purl.obolibrary.org/obo/DOID_0110781


A hereditary spastic paraplegia that has_material_basis_in mutation in the KIF1A gene on chromosome 2q37. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 30

Synonyms
  • SPG30
  • autosomal recessive spastic paraplegia 30
  • autosomal spastic paraplegia type 30
database cross reference
has obo namespace

disease_ontology

id

DOID:0110781