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Summary Literature (0)
MIM:612020 - SPASTIC PARAPLEGIA 39, AUTOSOMAL RECESSIVE; SPG39

Xenbase Genes: pnpla6

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012787 - hereditary spastic paraplegia 39

Disease Ontology (DO):
DOID:0110790 - hereditary spastic paraplegia 39