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Summary Literature (0)
MIM:601162 - SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A

Xenbase Genes: aldh18a1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011006 - hereditary spastic paraplegia 9A
MONDO:0015091 - autosomal dominant spastic paraplegia type 9

Disease Ontology (DO):
DOID:0110824 - hereditary spastic paraplegia 9A