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Traits

Traits linked to SLC51A

solute carrier family 51 member A

The Human Phenotype Ontology links 10 traits to SLC51A, by body system: features seen in people with one of the gene's rare conditions.

Laboratory abnormality

TraitHow often it is seen
Conjugated hyperbilirubinemiaAlways
Elevated alkaline phosphataseAlways
Elevated gamma-glutamyltransferase levelAlways
High liver enzymesAlways

Abnormality of the digestive system

TraitHow often it is seen
Chronic diarrheaAlways
Impaired release of bile from liverAlways
Periportal fibrosisAlways

Abnormality of blood and blood-forming tissues

TraitHow often it is seen
Bleeding requiring red cell transfusionAlways
Bruising susceptibilityAlways

Growth abnormality

TraitHow often it is seen
Faltering weightAlways

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 SLC51A and how often each is seen. Find out more at hpo.jax.org.

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