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Traits
Traits linked to FOXI3
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The Human Phenotype Ontology links 9 traits to FOXI3, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Small ears | Always |
| Abnormal shape/structure of ear | Very often (80–99%) |
| Cockleshell ear | Sometimes (5–29%) |
| Microtia, first degree | Sometimes (5–29%) |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Little lower jaw | Often (30–79%) |
| Bifid uvula | Sometimes (5–29%) |
| Submucous cleft palate | Sometimes (5–29%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Skin tags | Sometimes (5–29%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Dermal sinus tract | Sometimes (5–29%) |
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.
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to FOXI3 and how often each is seen. Find out more at hpo.jax.org.
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