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Metadata
ID	DOID:0110771
Name	hereditary spastic paraplegia 18
Definition	A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN2 gene on chromosome 8p11. https://www.ncbi.nlm.nih.gov/pubmed/21330303
Xrefs	GARD:4922 ICD10CM:G11.4 ORDO:209951
SKOS	exactMatch GARD:4922 exactMatch ORDO:209951 broadMatch ICD10CM:G11.4
Subsets	DO_rare_slim
Synonyms	SPG18 [EXACT]
Parent Relationships	is_a hereditary spastic paraplegia