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hereditary spastic paraplegia 18

Go to external page http://purl.obolibrary.org/obo/DOID_0110771

A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN2 gene on chromosome 8p11. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 18

Synonyms
  • IDMDC
  • SPG18
  • autosomal recessive spastic paraplegia 18
  • autosomal recessive spastic paraplegia type 18
  • intellectual disability, motor dysfunction and joint contractures
database cross reference
has obo namespace

disease_ontology

id

DOID:0110771