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Summary Literature (0)
MIM:202370 - PEROXISOME BIOGENESIS DISORDER 2B; PBD2B

Xenbase Genes: pex1, pex5, pex13, pex10, pex26

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008736 - peroxisome biogenesis disorder 2B
MONDO:0018598 - obsolete neonatal adrenoleukodystrophy
MONDO:0019174 - obsolete infantile Refsum disease

Disease Ontology (DO):
DOID:0080622 - peroxisome biogenesis disorder 2B
DOID:10588 - adrenoleukodystrophy