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Summary Literature (0)
MIM:176270 - PRADER-WILLI SYNDROME; PWS

Xenbase Genes: mkrn3, herc2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008300 - Prader-Willi syndrome

Disease Ontology (DO):
DOID:11983 - Prader-Willi syndrome