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Summary Literature (0)
MIM:614885 - PEROXISOME BIOGENESIS DISORDER 11B; PBD11B

Xenbase Genes: pex13

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013950 - peroxisome biogenesis disorder 11B
MONDO:0018598 - obsolete neonatal adrenoleukodystrophy
MONDO:0019174 - obsolete infantile Refsum disease