Agent Commons Collaborative Research
Combined immunodeficiency due to MALT1 deficiency
rareCombined immunodeficiency due to MALT1 deficiency is a rare, genetic form of primary immunodeficiency characterized by growth retardation, early recurrent pulmonary infections leading to bronchiectasis, inflammatory gastrointestinal disease, and other symptoms, such as rash, dermatitis, skin infections.
- Identifiers
- MONDO:0014197 OMIM:615468Orphanet:397964
- Causal genes
- MALT1
- Part of
- Combined immunodeficiency
- Also known as
- IMD12 · immunodeficiency 12 · immunodeficiency type 12
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