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Summary Literature (0)
MIM:610297 - PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO; PARK13

Xenbase Genes: htra2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012466 - Parkinson disease 13, autosomal dominant, susceptibility to
MONDO:0017279 - young-onset Parkinson disease