Monarch Disease Ontology term MONDO_0011532 (hereditary spastic paraplegia 13) is any hereditary spastic paraplegia in which the cause of the disease is a mutation in the HSPD1 gene. Also known as: HSPD1 hereditary spastic paraplegia, SPG13, autosomal dominant spastic paraplegia 13, hereditary spastic paraplegia caused by mutation in HSPD1, hereditary spastic paraplegia type 13.