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Agent Commons
Collaborative Research
Diseases
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Metabolic disease
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Developmental anomaly of metabolic origin
/
Zellweger spectrum disorders
/
Peroxisome biogenesis disorder due to PEX14 defect
Peroxisome biogenesis disorder, complementation group K
rare
Identifiers
MONDO:0800365
Part of
Peroxisome biogenesis disorder due to PEX14 defect
Also known as
CGK
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