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Summary Literature (0)
MIM:605280 - SPASTIC PARAPLEGIA 13, AUTOSOMAL DOMINANT; SPG13

Xenbase Genes: hspd1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011532 - hereditary spastic paraplegia 13

Disease Ontology (DO):
DOID:0110766 - hereditary spastic paraplegia 13