Trait
Iridocyclitis
A type of anterior uveitis, in which there is Inflammation of the iris and the ciliary body.
Summary
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test12 genes linked to Iridocyclitis
Changes in these genes cause rare conditions in which Iridocyclitis 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 |
|---|---|---|
| NOD2nucleotide binding oligomerization domain containing 2 | Very often (80–99%) | In 1 condition |
| FASFas cell surface death receptor | Often (30–79%) | In 1 condition |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Often (30–79%) | In 2 conditions |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Often (30–79%) | In 2 conditions |
| AIREautoimmune regulator | Sometimes (5–29%) | In 1 condition |
| ANKRD55ankyrin repeat domain 55 | Rarely (1–4%) | In 1 condition |
| CD247CD247 molecule | Rarely (1–4%) | In 1 condition |
| IL2RAinterleukin 2 receptor subunit alpha | Rarely (1–4%) | In 1 condition |
| IL2RBinterleukin 2 receptor subunit beta | Rarely (1–4%) | In 1 condition |
| PTPN2protein tyrosine phosphatase non-receptor type 2 | Rarely (1–4%) | In 1 condition |
| STAT4signal transducer and activator of transcription 4 | Rarely (1–4%) | In 1 condition |
| STUB1STIP1 homology and U-box containing protein 1 | Rarely (1–4%) | 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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