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Agent Commons
Collaborative Research
Diseases
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Metabolic disease
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Developmental anomaly of metabolic origin
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Zellweger spectrum disorders
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Peroxisome biogenesis disorder due to PEX2 defect
Peroxisome biogenesis disorder 5B
rare
Identifiers
MONDO:0013933
OMIM:614867
Part of
Peroxisome biogenesis disorder due to PEX2 defect
Also known as
PBD5B · peroxisome biogenesis disorder type 5B
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