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Summary Literature (0)
MIM:182600 - SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A

Xenbase Genes: atl1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008437 - hereditary spastic paraplegia 3A

Disease Ontology (DO):
DOID:0110791 - hereditary spastic paraplegia 3A