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Traits
Traits linked to CLCC1
chloride channel CLIC like 1
The Human Phenotype Ontology links 10 traits to CLCC1, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Decreased clarity of vision | Not recorded |
| Difficulties with night vision | Not recorded |
| Extreme sensitivity of the eyes to light | Not recorded |
| Optic disc pallor | Not recorded |
| Photoreceptor layer loss on macular OCT | Not recorded |
| Pigmentary retinopathy | Not recorded |
| Retina degeneration | Not recorded |
| Spicular pigmentation of the retina | Not recorded |
| Undetectable electroretinogram | Not recorded |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Narrowing of blood vessels in back of eye | Not 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 CLCC1 and how often each is seen. Find out more at hpo.jax.org.
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