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Summary Literature (0)
MIM:266510 - PEROXISOME BIOGENESIS DISORDER 3B; PBD3B

Xenbase Genes: pex1, pex2, pex26, pex12

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009959 - lumen of oropharynx
MONDO:0018598 - obsolete neonatal adrenoleukodystrophy
MONDO:0019174 - obsolete infantile Refsum disease

Disease Ontology (DO):
DOID:0050444 - infantile Refsum disease
DOID:0081241 - peroxisome biogenesis disorder 3B
DOID:10582 - Refsum disease