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Traits
Traits linked to DVL3
dishevelled segment polarity protein 3
The Human Phenotype Ontology links 105 traits to DVL3, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of head or neck
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Curvature of digit | Always |
| Disproportionately short middle portion of limb | Always |
| Short fingers or toes | Always |
| Short palm | Very often (80–99%) |
| Smaller or shorter than typical limbs | Very often (80–99%) |
| Curvature of little finger | Often (30–79%) |
| Short finger bones | Often (30–79%) |
| Avascular necrosis of the capital femoral epiphysis | Sometimes (5–29%) |
| Broad thumb | Sometimes (5–29%) |
| Coxa valga | Sometimes (5–29%) |
| Coxa vara | Sometimes (5–29%) |
| Elbow dislocation | Sometimes (5–29%) |
| Finger syndactyly | Sometimes (5–29%) |
| Hip dislocation | Sometimes (5–29%) |
| Permanent flexion of the finger | Sometimes (5–29%) |
| Webbed fingers or toes | Sometimes (5–29%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Short penis | Always |
| Undescended testes | Always |
| Underdeveloped penis | Very often (80–99%) |
| Small clitoris | Often (30–79%) |
| Small labia majora | Often (30–79%) |
| Underdeveloped inner lips | Often (30–79%) |
| Abnormality of the penis | Sometimes (5–29%) |
| Epispadias | Sometimes (5–29%) |
| Hypospadias | Sometimes (5–29%) |
| Vesicoureteral reflux | Sometimes (5–29%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Abnormal vertebral body morphology | Often (30–79%) |
| Funnel chest | Often (30–79%) |
| Hunched back | Often (30–79%) |
| Missing part of vertebrae | Often (30–79%) |
| Scoliosis | Often (30–79%) |
| Abnormal formation of the hip | Sometimes (5–29%) |
| Permanent flexion of the finger or toe | Sometimes (5–29%) |
| Pigeon chest | Sometimes (5–29%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Hole in heart wall separating two lower heart chambers | Often (30–79%) |
| Patent ductus arteriosus | Sometimes (5–29%) |
| Patent foramen ovale | Sometimes (5–29%) |
| Pulmonary artery atresia | Sometimes (5–29%) |
| Strawberry birthmark | Sometimes (5–29%) |
| Tricuspid regurgitation | Sometimes (5–29%) |
| Underdeveloped right heart | Sometimes (5–29%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Abnormal fingernail development | Sometimes (5–29%) |
| Hair loss | Sometimes (5–29%) |
| Overgrowth and curving of fingernail | Sometimes (5–29%) |
| Port-wine stain on eyelid | Sometimes (5–29%) |
| Ridged fingernail | Sometimes (5–29%) |
| Spinal dimple | Sometimes (5–29%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Umbilical hernia | Often (30–79%) |
| Anteriorly placed anus | Sometimes (5–29%) |
| Femoral hernia | Sometimes (5–29%) |
| Inguinal hernia | Sometimes (5–29%) |
| Omphalocele | Sometimes (5–29%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Wide-set eyes | Very often (80–99%) |
| Blue outer white part of eyeball | Often (30–79%) |
| Bulging eye | Often (30–79%) |
| Cross-eyed | Sometimes (5–29%) |
| Drooping upper eyelid | Sometimes (5–29%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Ears rotated toward back of head | Sometimes (5–29%) |
| Hearing impairment | Sometimes (5–29%) |
| Low-set ears | Sometimes (5–29%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Global developmental delay | Sometimes (5–29%) |
| Intellectual disability | Sometimes (5–29%) |
| Specific learning disability | Sometimes (5–29%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Short stature | Always |
| Severe short stature | 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 DVL3 and how often each is seen. Find out more at hpo.jax.org.
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