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Metadata
ID	DOID:0110821
Name	hereditary spastic paraplegia 76
Definition	A hereditary spastic paraplegia that has_material_basis_in mutation in the CAPN1 gene on chromosome 11q13. https://www.ncbi.nlm.nih.gov/pubmed/27153400
Xrefs	MIM:616907
Synonyms	autosomal recessive spastic paraplegia 76 [EXACT] SPG76 [EXACT]
Parent Relationships	is_a hereditary spastic paraplegia is_a autosomal recessive disease