Human Disease and Mouse Model Detail
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Human Disease
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Peroxisome Biogenesis Disorder 1B; PBD1B
OMIM ID: 601539
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Synonyms
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Adrenoleukodystrophy, Autosomal Neonatal;
Infantile Phytanic Acid Storage Disease;
Peroxisome Biogenesis Disorder (nald/Ird);
Peroxisome Biogenesis Disorder (neonatal Adrenoleukodystrophy/Infantile Refsum Disease);
Refsum Disease, Infantile
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Pex6
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PEX6*
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1:1 Homology
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Pex12
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PEX12*
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1:1 Homology
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Pex16
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PEX16*
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1:1 Homology
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Analysis Tools