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Summary Literature (0)
MIM:615043 - SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE; SPG43

Xenbase Genes: c4h19orf12

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014024 - hereditary spastic paraplegia 43

Disease Ontology (DO):
DOID:0110795 - hereditary spastic paraplegia 43