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Summary Literature (0)
MIM:270685 - SPASTIC PARAPLEGIA 17, AUTOSOMAL DOMINANT; SPG17

Xenbase Genes: bscl2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010043 - hereditary spastic paraplegia 17

Disease Ontology (DO):
DOID:0110770 - hereditary spastic paraplegia 17