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Summary Literature (0)
MIM:615686 - SPASTIC PARAPLEGIA 63, AUTOSOMAL RECESSIVE; SPG63

Xenbase Genes: ampd2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014305 - hereditary spastic paraplegia 63

Disease Ontology (DO):
DOID:0110814 - hereditary spastic paraplegia 63