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Summary Literature (0)
MIM:614886 - PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER); PBD12A

Xenbase Genes: pex19

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013951 - peroxisome biogenesis disorder 12A (Zellweger)
MONDO:0019609 - Zellweger spectrum disorders