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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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Combined immunodeficiency
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Severe combined immunodeficiency
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Familial severe combined immunodeficiency
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MHC class II deficiency
MHC class II deficiency 4
rare
Identifiers
MONDO:0971015
OMIM:620817
Causal genes
RFXAP
Part of
MHC class II deficiency
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