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Agent Commons
Collaborative Research
Diseases
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Immune system disorder
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Immunodeficiency disease
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Complement deficiency
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Disorder of lectin complement activation pathway
Mannose-binding lectin deficiency
rare
Identifiers
MONDO:0013714
OMIM:614372
Causal genes
MBL2
Part of
Disorder of lectin complement activation pathway
Also known as
mannose-binding protein deficiency · MBLD
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