Term Name:	hereditary spastic paraplegia 18A
Synonyms:	autosomal dominant spastic paraplegia 18, spastic paraplegia 18A
Definition:	A hereditary spastic paraplegia 18 that has_material_basis_in heterozygous mutation in the ERLIN2 gene on chromosome 8p11.
Ontology:	Human Disease [DOID:0070640]   ( DOID:0070640 )