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Traits
Traits linked to SNAI2
snail family transcriptional repressor 2
The Human Phenotype Ontology links 25 traits to SNAI2, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| White eyebrow | Often (30–79%) |
| White eyelashes | Often (30–79%) |
| Abnormality of cranium | Sometimes (5–29%) |
| Abnormally small head | Sometimes (5–29%) |
| Corners of eye widely separated | Sometimes (5–29%) |
| Long philtrum | Sometimes (5–29%) |
| Monobrow | Sometimes (5–29%) |
| Wide nasal bridge | Sometimes (5–29%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Loss of hair color | Very often (80–99%) |
| Piebald skin depigmentation | Very often (80–99%) |
| Premature graying of hair | Very often (80–99%) |
| White part of hair above forehead | Very often (80–99%) |
| Flat, discolored area of skin | Often (30–79%) |
| Patchy loss of skin color | Often (30–79%) |
| Skin cancer | Sometimes (5–29%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Hearing impairment | Very often (80–99%) |
| Sensorineural hearing impairment | Often (30–79%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Different colored eyes | Often (30–79%) |
| Drooping upper eyelid | Sometimes (5–29%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Ataxia | Sometimes (5–29%) |
| Intellectual disability | Sometimes (5–29%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Abnormality of lung artery | Sometimes (5–29%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Enlarged colon lacking nerve cells | Sometimes (5–29%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Abnormality of the kidney | Sometimes (5–29%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Low muscle tone | 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 SNAI2 and how often each is seen. Find out more at hpo.jax.org.
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