Term Name:	hereditary spastic paraplegia 11
Synonyms:	autosomal recessive spastic paraplegia 11, autosomal recessive spastic paraplegia complicated with thin corpus callosum, autosomal recessive spastic paraplegia type 11, autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum, HSP-TCC, Nakamura-Osame syndrome, spastic paraplegia-intellectual disability-thin corpus callosum syndrome, SPG11
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the SPG11 gene on chromosome 15q21.
Ontology:	Human Disease [DOID:0110764]   ( DOID:0110764 )