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Traits
Traits linked to WDR37
WD repeat domain 37
The Human Phenotype Ontology links 27 traits to WDR37, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Downturned corners of mouth | Always |
| Prominent nasal bridge | Always |
| Smooth philtrum | Always |
| High forehead | Very often (80–99%) |
| Development of small head that was not present at birth | Often (30–79%) |
| Eye folds | Often (30–79%) |
| Redundant neck skin | Often (30–79%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| An opening in the wall separating the top two chambers of the heart | Often (30–79%) |
| Hole in heart wall separating two lower heart chambers | Often (30–79%) |
| Patent ductus arteriosus | Often (30–79%) |
| Enlarged heart | Sometimes (5–29%) |
| Patent foramen ovale | Sometimes (5–29%) |
| Tricuspid regurgitation | Sometimes (5–29%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Absent speech development | Always |
| Epilepsy | Always |
| Global developmental delay | Always |
| Intellectual disability | Always |
| Abnormality of the cerebellum | Not recorded |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Notched pupil | Very often (80–99%) |
| Abnormally small eyeball | Often (30–79%) |
| Wide-set eyes | Often (30–79%) |
| Peters anomaly | Sometimes (5–29%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Low-set ears | Often (30–79%) |
| Sensorineural hearing impairment | Often (30–79%) |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Abnormality of the palm lines | Always |
Abnormality of the breast
| Trait | How often it is seen |
|---|---|
| Wide-spaced nipples | Often (30–79%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Bilateral cryptorchidism | Always |
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 WDR37 and how often each is seen. Find out more at hpo.jax.org.
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