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Human Disease and Mouse Model Detail
Human Disease Peroxisome Biogenesis Disorder 1B; PBD1B
OMIM ID: 601539
Human Phenotype Ontology associations
Synonyms Adrenoleukodystrophy, Autosomal Neonatal; Infantile Phytanic Acid Storage Disease; Peroxisome Biogenesis Disorder; Peroxisome Biogenesis Disorder (nald/Ird); Peroxisome Biogenesis Disorder (neonatal Adrenoleukodystrophy/Infantile Refsum Disease); Refsum Disease, Infantile
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     PEX1* Pex1   HomoloGene and HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory