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Traits
Traits linked to SLC10A1
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The Human Phenotype Ontology links 4 traits to SLC10A1, by body system: features seen in people with one of the gene's rare conditions.
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Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Deficient in vitamin D | Always |
| Increased serum bile acid concentration | Always |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Prolonged yellowing of skin in newborn | Always |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Osteopenia | Often (30–79%) |
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 SLC10A1 and how often each is seen. Find out more at hpo.jax.org.
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