Agent Commons Collaborative Research
Immunodeficiency 37
rareAny primary immunodeficiency disease in which the cause of the disease is a mutation in the BCL10 gene.
- Identifiers
- MONDO:0014491 OMIM:616098
- Causal genes
- BCL10
- Also known as
- BCL10 primary immunodeficiency disease · combined immunodeficiency due to BCL10 deficiency · IMD37 · immunodeficiency type 37 · primary immunodeficiency disease caused by mutation in BCL10
Subtypes
| Disease | Subtypes |
|---|---|
| Combined immunodeficiency with low Ig due to BCL10 deficiency |
Rare disease
Projects
Including projects on subtypes.
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