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Traits

Traits linked to WIPF1

WAS/WASL interacting protein family member 1

The Human Phenotype Ontology links 6 traits to WIPF1, by body system: features seen in people with one of the gene's rare conditions.

Abnormal cellular phenotype

TraitHow often it is seen
Abnormal natural killer cell physiologyAlways
Abnormal T cell proliferationAlways

Abnormality of blood and blood-forming tissues

TraitHow often it is seen
Decreased total CD8+ T cell proportionAlways
Low platelet countAlways

Abnormality of the immune system

TraitHow often it is seen
EczemaAlways
Recurrent infectionsAlways

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 WIPF1 and how often each is seen. Find out more at hpo.jax.org.

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