Term Name:	hereditary spastic paraplegia 61
Synonyms:	autosomal recessive spastic paraplegia 61, autosomal recessive spastic paraplegia type 61, SPG61
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the ARL6IP1 gene on chromosome 16p12.
Ontology:	Human Disease [DOID:0110812]   ( DOID:0110812 )