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Summary Literature (0)
MIM:613647 - SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48

Xenbase Genes: ap5z1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013342 - hereditary spastic paraplegia 48

Disease Ontology (DO):
DOID:0110800 - hereditary spastic paraplegia 48