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Summary Literature (0)
MIM:603563 - SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT; SPG8

Xenbase Genes: washc5

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011339 - hereditary spastic paraplegia 8

Disease Ontology (DO):
DOID:0110823 - hereditary spastic paraplegia 8