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MIM:601539 - PEROXISOME BIOGENESIS DISORDER 1B; PBD1B
Xenbase Genes: pex1
Human Disease Resource: MIM
| MONDO:0011101 - peroxisome biogenesis disorder 1B |
| MONDO:0018598 - obsolete neonatal adrenoleukodystrophy |
| MONDO:0019174 - obsolete infantile Refsum disease |
| DOID:0081240 - peroxisome biogenesis disorder 1B |
