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Summary Literature (0)
MIM:612539 - SPASTIC PARAPLEGIA 42, AUTOSOMAL DOMINANT; SPG42

Xenbase Genes: slc33a1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012928 - hereditary spastic paraplegia 42

Disease Ontology (DO):
DOID:0110794 - hereditary spastic paraplegia 42