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Summary Literature (0)
MIM:611225 - SPASTIC PARAPLEGIA 18B, AUTOSOMAL RECESSIVE; SPG18B

Xenbase Genes: erlin2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012639 - hereditary spastic paraplegia 18

Disease Ontology (DO):
DOID:0110771 - hereditary spastic paraplegia 18