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Summary Literature (0)
MIM:611252 - SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE; SPG32

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012643 - hereditary spastic paraplegia 32

Disease Ontology (DO):
DOID:0110783 - hereditary spastic paraplegia 32