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Summary Literature (0)
MIM:604805 - SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT; SPG12

Xenbase Genes: rtn2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011489 - hereditary spastic paraplegia 12

Disease Ontology (DO):
DOID:0110765 - hereditary spastic paraplegia 12