Trait
Posterior uveitis
Inflammation of the uveal tract in which the primary site of inflammation is the retina or choroid.
Summary
- Also called
- Choroiditis
Reference genomeGRCh38hg38
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Get my Genome Test6 genes linked to Posterior uveitis
Changes in these genes cause rare conditions in which Posterior uveitis 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 |
| BCL10BCL10 immune signaling adaptor | Sometimes (5–29%) | In 1 condition |
| BIRC3baculoviral IAP repeat containing 3 | Sometimes (5–29%) | In 1 condition |
| FOXP1forkhead box P1 | Sometimes (5–29%) | In 1 condition |
| IGHimmunoglobulin heavy locus | Sometimes (5–29%) | In 1 condition |
| MALT1MALT1 paracaspase | Sometimes (5–29%) | 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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