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Summary Literature (0)
MIM:606693 - KUFOR-RAKEB SYNDROME; KRS

Xenbase Genes: atp13a2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011706 - Kufor-Rakeb syndrome
MONDO:0017809 - parkinsonism due to ATP13A2 deficiency

Disease Ontology (DO):
DOID:0060556 - Kufor-Rakeb syndrome