Trait
Recurrent abscess formation
An increased susceptibility to abscess formation, as manifested by a medical history of recurrent abscesses.
Summary
- Body system
- Abnormality of the immune system
Reference genomeGRCh38hg38
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Get my Genome Test11 genes linked to Recurrent abscess formation
Changes in these genes cause rare conditions in which Recurrent abscess formation is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| CEBPECCAAT enhancer binding protein epsilon | Always | In 1 condition |
| NCF2neutrophil cytosolic factor 2 | Always | In 1 condition |
| AP3B1adaptor related protein complex 3 subunit beta 1 | Often (30–79%) | In 1 condition |
| CD247CD247 molecule | Sometimes (5–29%) | In 1 condition |
| CD3DCD3 delta subunit of T-cell receptor complex | Sometimes (5–29%) | In 1 condition |
| CD3ECD3 epsilon subunit of T-cell receptor complex | Sometimes (5–29%) | In 1 condition |
| PI4KAphosphatidylinositol 4-kinase alpha | Sometimes (5–29%) | In 1 condition |
| SP110SP110 nuclear body protein | Sometimes (5–29%) | In 1 condition |
| SYKspleen associated tyrosine kinase | Sometimes (5–29%) | In 1 condition |
| TTC7Atetratricopeptide repeat domain 7A | Sometimes (5–29%) | In 1 condition |
| FCN3ficolin 3 | Not recorded | In 1 condition |
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.
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Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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