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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 PEX13 defect
Peroxisome biogenesis disorder 11B
rare
Identifiers
MONDO:0013950
OMIM:614885
Part of
Peroxisome biogenesis disorder due to PEX13 defect
Also known as
PBD11B · peroxisome biogenesis disorder type 11B
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