Term Name:	hereditary spastic paraplegia 15
Synonyms:	autosomal recessive spastic paraplegia 15, autosomal recessive spastic paraplegia type 15, hereditary spastic paraparesis type 15, Kjellin syndrome, spastic paraplegia and retinal degeneration, spastic paraplegia-retinal degeneration syndrome, SPG15
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the ZFYVE26 gene on chromosome 14q24.1.
Ontology:	Human Disease [DOID:0110768]   ( DOID:0110768 )