Immunodeficiency 19

MONDO:0014280

Any 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

2 clinical trials for this condition and its sub-types, 0 tagged with Immunodeficiency 19 itself.

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Part of

↑ Familial severe combined immunodeficiency (22) ↑ T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta (0)

Including sub-types (2) Tagged with Immunodeficiency 19 (0)

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