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Immunodeficiency 19
MONDO:0014280Any severe combined immunodeficiency in which the cause of the disease is a mutation in the CD3D gene.
Also known as: CD3D severe combined immunodeficiency (disease), CD3delta deficiency, immunodeficiency 19, immunodeficiency type 19, severe combined immunodeficiency (disease) caused by mutation in CD3D, CD3-Delta deficiency, IMD19, SCID, T cell-negative, B cell-positive, NK cell-positive
16 clinical trials for this condition and its sub-types.
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Immune system disorder
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Immunodeficiency disease
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Severe combined immunodeficiency
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Human disease
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Combined immunodeficiency
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Disease of genetic or genomic mechanism
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