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Traits
Traits linked to SLC27A4
solute carrier family 27 member 4
The Human Phenotype Ontology links 19 traits to SLC27A4, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Follicular hyperkeratosis | Always |
| Generalized ichthyosis | Always |
| Itching | Always |
| Thickening of upper layer of skin | Always |
| Ichthyosis | Very often (80–99%) |
| Patchy darkened skin | Not recorded |
Abnormality of prenatal development or birth
| Trait | How often it is seen |
|---|---|
| Caseous vernix-like desquamation | Always |
| High levels of amniotic fluid | Always |
| Premature birth | Always |
| Desquamation of skin soon after birth | Very often (80–99%) |
Abnormality of the immune system
| Trait | How often it is seen |
|---|---|
| Red scaly skin caused by inflammatory skin disease | Always |
| Asthma | Sometimes (5–29%) |
| Food allergy | Sometimes (5–29%) |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Absence of scalp hair | Sometimes (5–29%) |
| Hay fever | Sometimes (5–29%) |
Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Neonatal asphyxia | Always |
| Neonatal respiratory distress | Very often (80–99%) |
Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| High blood eosinophil count | Very often (80–99%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Skin writing | Not recorded |
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 SLC27A4 and how often each is seen. Find out more at hpo.jax.org.
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