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Summary Literature (0)
OMIM:605280 - SPASTIC PARAPLEGIA 13, AUTOSOMAL DOMINANT; SPG13

In Disease Ontology (DO):
DOID:0110766 - hereditary spastic paraplegia 13

In Mondo Disease Ontology:
MONDO:0011532 - hereditary spastic paraplegia 13

Human Disease Resources: OMIM

Xenbase Genes: hspd1