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Summary Literature (1)
MIM:182601 - SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4

Xenbase Genes: spast

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008438 - hereditary spastic paraplegia 4

Disease Ontology (DO):
DOID:0110792 - hereditary spastic paraplegia 4