Terminology Service for NFDI4Health

hereditary spastic paraplegia 61

Go to external page http://purl.obolibrary.org/obo/DOID_0110812


A hereditary spastic paraplegia that has_material_basis_in mutation in the ARL6IP1 gene on chromosome 16p12. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 61

Synonyms
  • SPG61
  • autosomal recessive spastic paraplegia 61
  • autosomal recessive spastic paraplegia type 61
database cross reference
has obo namespace

disease_ontology

id

DOID:0110812