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Metadata
ID	DOID:0110766
Name	hereditary spastic paraplegia 13
Definition	A hereditary spastic paraplegia that is characterized by a pure form of the disease with late onset and has_material_basis_in mutation in the HSPD1 gene on chromosome 2q33. https://www.ncbi.nlm.nih.gov/pubmed/11898127
Xrefs	GARD:9616 ICD10CM:G11.4 MIM:605280 ORDO:100994
Subsets	DO_rare_slim
Synonyms	autosomal dominant spastic paraplegia 13 [EXACT] SPG13 [EXACT]
Parent Relationships	is_a hereditary spastic paraplegia is_a autosomal dominant disease