Terminology Service for NFDI4Health

hereditary spastic paraplegia 62

Go to external page http://purl.obolibrary.org/obo/DOID_0110813


A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN1 gene on chromosome 10q24. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 62

Synonyms
  • SPG62
  • autosomal recessive spastic paraplegia 62
  • autosomal recessive spastic paraplegia type 62
database cross reference
has obo namespace

disease_ontology

id

DOID:0110813