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Traits

Traits linked to ROR1

ROR family WNT receptor 1

The Human Phenotype Ontology links 2 traits to ROR1, by body system: features seen in people with one of the gene's rare conditions.

Abnormality of the ear

TraitHow often it is seen
Congenital sensorineural hearing impairmentAlways

Abnormality of the eye

TraitHow often it is seen
Cat eyeOften (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 ROR1 and how often each is seen. Find out more at hpo.jax.org.

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