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Summary Literature (0)
MIM:619686 - SPASTIC PARAPLEGIA 85, AUTOSOMAL RECESSIVE; SPG85


Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0030512 - spastic paraplegia 85, autosomal recessive

Disease Ontology (DO):
DOID:0112345 - hereditary spastic paraplegia 85