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Summary Literature (0)
MIM:610250 - SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT; SPG31

Xenbase Genes: reep1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012453 - hereditary spastic paraplegia 31

Disease Ontology (DO):
DOID:0110782 - hereditary spastic paraplegia 31