Term Name:	hereditary spastic paraplegia 62
Synonyms:	autosomal recessive spastic paraplegia 62, autosomal recessive spastic paraplegia type 62, SPG62
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN1 gene on chromosome 10q24.
Ontology:	Human Disease [DOID:0110813]   ( DOID:0110813 )