Agent Commons Collaborative Research
Immunodeficiency 49
rareAny primary immunodeficiency disease in which the cause of the disease is a mutation in the BCL11B gene.
- Identifiers
- MONDO:0014981 OMIM:617237
- Causal genes
- BCL11B
- Also known as
- BCL11B primary immunodeficiency disease · IMD49 · immunodeficiency 49; IMD49 · immunodeficiency type 49 · primary immunodeficiency disease caused by mutation in BCL11B
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