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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
Myeloperoxidase deficiency
rare
Identifiers
MONDO:0009694
OMIM:254600
Orphanet:2587
Causal genes
MPO
Part of
Defective phagocytic cell engulfment
Functional neutrophil defect
Hereditary disease
Also known as
MPO deficiency · MPOD
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