Trait
Conjunctival hyperemia
Dilatation of the blood vessels of the conjunctiva leading to a red appearance of the sclera.
Summary
- Also called
- Conjunctival hyperaemia, Conjunctival injection, Conjunctival vascular congestion
Read the genes linked to Conjunctival hyperemia, and the rest of your genome, with one test.
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Get my Genome Test8 genes linked to Conjunctival hyperemia
Changes in these genes cause rare conditions in which Conjunctival hyperemia 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 |
|---|---|---|
| NLRP3NLR family pyrin domain containing 3 | Always | In 2 conditions |
| AP1G1adaptor related protein complex 1 subunit gamma 1 | Often (30–79%) | 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 1 condition |
| MAPTmicrotubule associated protein tau | Often (30–79%) | In 1 condition |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Often (30–79%) | In 1 condition |
| SHMT2serine hydroxymethyltransferase 2 | Often (30–79%) | In 1 condition |
| TNFRSF1ATNF receptor superfamily member 1A | Often (30–79%) | 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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