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Traits

Traits linked to CHRDL1

chordin like 1

The Human Phenotype Ontology links 14 traits to CHRDL1, by body system: features seen in people with one of the gene's rare conditions.

Abnormality of the eye

TraitHow often it is seen
Decreased clarity of visionAlways
Enlarged corneaAlways
Iris transillumination defectAlways
Corneal arcusOften (30–79%)
Retinal detachmentSometimes (5–29%)
AstigmatismNot recorded
Clouding of the lens of the eyeNot recorded
Constricted pupilsNot recorded
Deep anterior chamberNot recorded
GlaucomaNot recorded
IridodonesisNot recorded
Mosaic corneal dystrophyNot recorded
Partially dislocated lensNot recorded
Thin corneaNot 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 CHRDL1 and how often each is seen. Find out more at hpo.jax.org.

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