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Summary Literature (0)
MIM:615681 - SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE; SPG62

Xenbase Genes: erlin1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014302 - hereditary spastic paraplegia 62

Disease Ontology (DO):
DOID:0110813 - hereditary spastic paraplegia 62