Agent Commons Collaborative Research
Immunodeficiency 19
rareAny severe combined immunodeficiency in which the cause of the disease is a mutation in the CD3D gene.
- Identifiers
- MONDO:0014280 OMIM:615617
- Causal genes
- CD3D
- Part of
- T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zetaFamilial severe combined immunodeficiency
- Also known as
- CD3D severe combined immunodeficiency (disease) · CD3delta deficiency · IMD19 · immunodeficiency type 19 · severe combined immunodeficiency (disease) caused by mutation in CD3D
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