Who We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
Traits
Traits linked to RD3
RD3 regulator of GUCY2D
The Human Phenotype Ontology links 27 traits to RD3, by body system: features seen in people with one of the gene's rare conditions.
Who We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
Who We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Abnormal optic disc morphology | Very often (80–99%) |
| Abnormal retinal pigmentation | Very often (80–99%) |
| Marked vision impairment | Very often (80–99%) |
| Abnormal electroretinogram | Often (30–79%) |
| Abnormal full-field electroretinogram | Often (30–79%) |
| Bulging cornea | Often (30–79%) |
| Clouding of the lens of the eye | Often (30–79%) |
| Extreme sensitivity of the eyes to light | Often (30–79%) |
| Farsightedness | Often (30–79%) |
| Involuntary, rapid, rhythmic eye movements | Often (30–79%) |
| Slow pupillary light response | Often (30–79%) |
| Optic disc drusen | Sometimes (5–29%) |
| Optic disc pallor | Sometimes (5–29%) |
| Abnormal macular pigmentation | Not recorded |
| Blindness present at birth | Not recorded |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Abnormality of neuronal migration | Often (30–79%) |
| Aplasia/Hypoplasia of the cerebellar vermis | Often (30–79%) |
| Epilepsy | Often (30–79%) |
| Eye poking | Often (30–79%) |
| Paralysis or weakness of one side of body | Often (30–79%) |
| Autism spectrum disorder | Sometimes (5–29%) |
| Global developmental delay | Sometimes (5–29%) |
| Intellectual disability | Sometimes (5–29%) |
| Motor delay | Sometimes (5–29%) |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Encephalocele | Often (30–79%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Hearing impairment | Sometimes (5–29%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Low muscle tone | Often (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 RD3 and how often each is seen. Find out more at hpo.jax.org.
Who We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks