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Traits
Traits linked to CEBPE
CCAAT enhancer binding protein epsilon
The Human Phenotype Ontology links 18 traits to CEBPE, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Absent neutrophil specific granules | Always |
| Bloody nose | Always |
| Hyposegmentation of neutrophil nuclei | Always |
| Impaired neutrophil bactericidal activity | Always |
| Impaired neutrophil chemotaxis | Always |
| Absent neutrophil lactoferrin | Not recorded |
| Increased neutrophil mitochondria | Not recorded |
| Increased neutrophil ribosomes | Not recorded |
Abnormality of the immune system
| Trait | How often it is seen |
|---|---|
| Recurrent abscess formation | Always |
| Recurrent bacterial infections | Always |
| Recurrent pneumonia | Always |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Episodic fever | Always |
| Low neutrophil alkaline phosphatase | Always |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Recurrent canker sores | Always |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Abdominal pain | Always |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Recurrent middle ear infection | Always |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Paronychia | Always |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Neutrophil nuclear clefts | Not recorded |
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 CEBPE and how often each is seen. Find out more at hpo.jax.org.
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