Term Name:	hereditary spastic paraplegia 18
Synonyms:	autosomal recessive spastic paraplegia 18, autosomal recessive spastic paraplegia type 18, IDMDC, intellectual disability, motor dysfunction and joint contractures, SPG18
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN2 gene on chromosome 8p11.
Ontology:	Human Disease [DOID:0110771]   ( DOID:0110771 )