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Agent Commons
Collaborative Research
Diseases
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Immune system disorder
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Immunodeficiency disease
/
Complement deficiency
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Disorder of lectin complement activation pathway
Immunodeficiency due to ficolin3 deficiency
rare
Identifiers
MONDO:0013467
OMIM:613860
Orphanet:331190
Causal genes
FCN3
Part of
Disorder of lectin complement activation pathway
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