Trait
Pus-filled lesion
Clinical name: Pyoderma
Any manifestation of a skin disease associated with the production of pus.
Summary
Reference genomeGRCh38hg38
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Get my Genome Test7 genes linked to Pus-filled lesion
Changes in these genes cause rare conditions in which Pus-filled lesion 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 |
|---|---|---|
| IL10RAinterleukin 10 receptor subunit alpha | Always | In 1 condition |
| TRAF3TNF receptor associated factor 3 | Always | In 1 condition |
| LAMA3laminin subunit alpha 3 | Rarely (1–4%) | In 1 condition |
| LAMB3laminin subunit beta 3 | Rarely (1–4%) | In 1 condition |
| LAMC2laminin subunit gamma 2 | Rarely (1–4%) | In 1 condition |
| BTKBruton tyrosine kinase | Not recorded | In 2 conditions |
| FOXN1forkhead box N1 | 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.
Broader traits
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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