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Traits
Traits linked to ROR2
ROR family WNT receptor 2
The Human Phenotype Ontology links 151 traits to ROR2, 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
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Missing part of vertebrae | Very often (80–99%) |
| Rib fusion | Very often (80–99%) |
| Vertebral segmentation defect | Very often (80–99%) |
| Double-Jointed | Often (30–79%) |
| Funnel chest | Often (30–79%) |
| Hunched back | Often (30–79%) |
| Scoliosis | Often (30–79%) |
| Abnormality of the hip bone | Sometimes (5–29%) |
| Permanent flexion of the finger or toe | Sometimes (5–29%) |
| Pigeon chest | Sometimes (5–29%) |
| Delayed bone maturation | Not recorded |
| Missing ribs | Not recorded |
| Short long bone | Not recorded |
| Small sacrum | Not recorded |
| Thoracic hemivertebrae | Not recorded |
| Thoracolumbar scoliosis | Not recorded |
| Vertebral fusion | Not recorded |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Short penis | Always |
| Underdeveloped penis | Very often (80–99%) |
| Hydronephrosis | Often (30–79%) |
| Increased calcium level in kidney | Often (30–79%) |
| Kidney stone | Often (30–79%) |
| Underdeveloped female external genitalia | Often (30–79%) |
| Underdeveloped inner lips | Often (30–79%) |
| Undescended testes | Often (30–79%) |
| Hypospadias | Sometimes (5–29%) |
| Multicystic kidney dysplasia | Sometimes (5–29%) |
| Small labia majora | Sometimes (5–29%) |
| Small clitoris | Not recorded |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Small nail | Always |
| Abnormal fingernail development | Often (30–79%) |
| Atypical nail growth | Often (30–79%) |
| Beauty mark | Sometimes (5–29%) |
| Hair loss | Sometimes (5–29%) |
| port-wine stain | Sometimes (5–29%) |
| Spinal dimple | Sometimes (5–29%) |
| Absent nails | Not recorded |
| Small fingernail | Not recorded |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Abnormal aortic morphology | Sometimes (5–29%) |
| Abnormal pulmonary valve morphology | Sometimes (5–29%) |
| Abnormal tricuspid valve morphology | Sometimes (5–29%) |
| Abnormality of the heart | Sometimes (5–29%) |
| An opening in the wall separating the top two chambers of the heart | Sometimes (5–29%) |
| Hole in heart wall separating two lower heart chambers | Sometimes (5–29%) |
| Tetralogy of Fallot | Sometimes (5–29%) |
| Right ventricular outlet tract obstruction | Not recorded |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Chronic infections of the middle ear | Often (30–79%) |
| Ears rotated toward back of head | Often (30–79%) |
| Hearing impairment | Often (30–79%) |
| Low-set ears | Often (30–79%) |
| Small ears | Sometimes (5–29%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Wide-set eyes | Very often (80–99%) |
| Bulging eye | Often (30–79%) |
| Blue outer white part of eyeball | Sometimes (5–29%) |
| Cross-eyed | Sometimes (5–29%) |
| Drooping upper eyelid | Sometimes (5–29%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Umbilical hernia | Often (30–79%) |
| Abnormal anus position | Sometimes (5–29%) |
| Inguinal hernia | Sometimes (5–29%) |
| Extra kidney | Not recorded |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Intellectual disability | Sometimes (5–29%) |
| Global developmental delay | Not recorded |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Short stature | Always |
| Disproportionate short-limb short stature | Very often (80–99%) |
Abnormality of the immune system
| Trait | How often it is seen |
|---|---|
| Recurrent respiratory infections | Sometimes (5–29%) |
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 ROR2 and how often each is seen. Find out more at hpo.jax.org.
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