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MIM:266510 - PEROXISOME BIOGENESIS DISORDER 3B; PBD3B
Xenbase Genes: pex1, pex2, pex26, pex12
Human Disease Resource: MIM
MONDO:0009959 - peroxisome biogenesis disorder type 3B |
MONDO:0018598 - obsolete neonatal adrenoleukodystrophy |
MONDO:0019174 - obsolete infantile Refsum disease |
DOID:0050444 - infantile Refsum disease |
DOID:0081241 - peroxisome biogenesis disorder 3B |
DOID:10582 - Refsum disease |