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Traits
Traits linked to CARD11
caspase recruitment domain family member 11
The Human Phenotype Ontology links 27 traits to CARD11, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the immune system
| Trait | How often it is seen |
|---|---|
| Baby eczema | Always |
| Decreased immune function | Always |
| Decreased specific antibody response to unconjugated polysaccharide vaccine | Always |
| Pneumocystis jirovecii pneumonia | Always |
| Recurrent infections | Always |
| Recurrent respiratory infections | Always |
| Asthma | Often (30–79%) |
| Food allergy | Often (30–79%) |
| Pneumonia | Often (30–79%) |
| Disseminated molluscum contagiosum | Sometimes (5–29%) |
| Severe cytomegalovirus infection | Sometimes (5–29%) |
Abnormal cellular phenotype
| Trait | How often it is seen |
|---|---|
| Agammaglobulinemia | Always |
| Decreased antigen-specific T cell proliferation | Always |
| Decreased circulating antibody level | Always |
| Decreased circulating IgA concentration | Always |
| Decreased circulating IgM concentration | Often (30–79%) |
| Increased circulating IgE concentration | Often (30–79%) |
Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Decreased regulatory T cell proportion | Always |
| Increased total B cell count | Always |
| Low blood monocyte number | Always |
| Lymphoid hyperplasia | Always |
| High blood eosinophil count | Very often (80–99%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Chronic diarrhea | Sometimes (5–29%) |
| Colonic eosinophilia | Sometimes (5–29%) |
| Ulcerative colitis | Sometimes (5–29%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Increased spleen size | Always |
Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Permanent enlargement of the airways of the lungs | Sometimes (5–29%) |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to CARD11 and how often each is seen. Find out more at hpo.jax.org.
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