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Metadata
ID	DOID:0110822
Name	hereditary spastic paraplegia 77
Definition	A hereditary spastic paraplegia that has_material_basis_in mutation in the FARS2 gene on chromosome 6p25. https://www.ncbi.nlm.nih.gov/pubmed/26553276
Xrefs	ICD10CM:G11.4 OMIM:617046 ORDO:466722
Subsets	DO_rare_slim
Synonyms	autosomal recessive spastic paraplegia 77 [EXACT] SPG77 [EXACT]
Parent Relationships	is_a hereditary spastic paraplegia is_a autosomal recessive disease