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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 PEX3 defect
Peroxisome biogenesis disorder 10B
rare
Identifiers
MONDO:0054549
OMIM:617370
Part of
Peroxisome biogenesis disorder due to PEX3 defect
Also known as
PBD10B
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