Cui ne adresămȘtiința noastrăProduseRezultate
ConectareÎntrebațiSecvențiați-vă genomul↗
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.
Cui ne adresămȘtiința noastrăProduseRezultate
ConectareÎntrebațiSecvențiați-vă genomul↗
Cui ne adresămȘtiința noastrăProduseRezultate
ConectareÎntrebațiSecvențiați-vă genomul↗
Abnormality of head or neck
Abnormality of limbs
Abnormality of the musculoskeletal system
| Trait | Cât de frecvent apare |
|---|---|
| Missing part of vertebrae | Foarte des (80–99%) |
| Rib fusion | Foarte des (80–99%) |
| Vertebral segmentation defect | Foarte des (80–99%) |
| Double-Jointed | Des (30–79%) |
| Funnel chest | Des (30–79%) |
| Hunched back | Des (30–79%) |
| Scoliosis | Des (30–79%) |
| Abnormality of the hip bone | Uneori (5–29%) |
| Permanent flexion of the finger or toe | Uneori (5–29%) |
| Pigeon chest | Uneori (5–29%) |
| Delayed bone maturation | Neînregistrat |
| Missing ribs | Neînregistrat |
| Short long bone | Neînregistrat |
| Small sacrum | Neînregistrat |
| Thoracic hemivertebrae | Neînregistrat |
| Thoracolumbar scoliosis | Neînregistrat |
| Vertebral fusion | Neînregistrat |
Abnormality of the genitourinary system
| Trait | Cât de frecvent apare |
|---|---|
| Short penis | Întotdeauna |
| Underdeveloped penis | Foarte des (80–99%) |
| Hydronephrosis | Des (30–79%) |
| Increased calcium level in kidney | Des (30–79%) |
| Kidney stone | Des (30–79%) |
| Underdeveloped female external genitalia | Des (30–79%) |
| Underdeveloped inner lips | Des (30–79%) |
| Undescended testes | Des (30–79%) |
| Hypospadias | Uneori (5–29%) |
| Multicystic kidney dysplasia | Uneori (5–29%) |
| Small labia majora | Uneori (5–29%) |
| Small clitoris | Neînregistrat |
Abnormality of the integument
| Trait | Cât de frecvent apare |
|---|---|
| Small nail | Întotdeauna |
| Abnormal fingernail development | Des (30–79%) |
| Atypical nail growth | Des (30–79%) |
| Beauty mark | Uneori (5–29%) |
| Hair loss | Uneori (5–29%) |
| port-wine stain | Uneori (5–29%) |
| Spinal dimple | Uneori (5–29%) |
| Absent nails | Neînregistrat |
| Small fingernail | Neînregistrat |
Abnormality of the cardiovascular system
| Trait | Cât de frecvent apare |
|---|---|
| Abnormal aortic morphology | Uneori (5–29%) |
| Abnormal pulmonary valve morphology | Uneori (5–29%) |
| Abnormal tricuspid valve morphology | Uneori (5–29%) |
| Abnormality of the heart | Uneori (5–29%) |
| An opening in the wall separating the top two chambers of the heart | Uneori (5–29%) |
| Hole in heart wall separating two lower heart chambers | Uneori (5–29%) |
| Tetralogy of Fallot | Uneori (5–29%) |
| Right ventricular outlet tract obstruction | Neînregistrat |
Abnormality of the ear
| Trait | Cât de frecvent apare |
|---|---|
| Chronic infections of the middle ear | Des (30–79%) |
| Ears rotated toward back of head | Des (30–79%) |
| Hearing impairment | Des (30–79%) |
| Low-set ears | Des (30–79%) |
| Small ears | Uneori (5–29%) |
Abnormality of the eye
| Trait | Cât de frecvent apare |
|---|---|
| Wide-set eyes | Foarte des (80–99%) |
| Bulging eye | Des (30–79%) |
| Blue outer white part of eyeball | Uneori (5–29%) |
| Cross-eyed | Uneori (5–29%) |
| Drooping upper eyelid | Uneori (5–29%) |
Abnormality of the digestive system
| Trait | Cât de frecvent apare |
|---|---|
| Umbilical hernia | Des (30–79%) |
| Abnormal anus position | Uneori (5–29%) |
| Inguinal hernia | Uneori (5–29%) |
| Extra kidney | Neînregistrat |
Abnormality of the nervous system
| Trait | Cât de frecvent apare |
|---|---|
| Intellectual disability | Uneori (5–29%) |
| Global developmental delay | Neînregistrat |
Growth abnormality
| Trait | Cât de frecvent apare |
|---|---|
| Short stature | Întotdeauna |
| Disproportionate short-limb short stature | Foarte des (80–99%) |
Abnormality of the immune system
| Trait | Cât de frecvent apare |
|---|---|
| Recurrent respiratory infections | Uneori (5–29%) |
Cât de frecvent apare în rândul persoanelor cu una dintre afecțiunile asociate genei, cel mai des întâlnit dintre acestea, conform Human Phenotype Ontology. Aceste pagini descriu trăsături și cercetările din spatele lor; ele nu reprezintă un diagnostic, iar pentru simptome trebuie să vă adresați medicului sau consilierului genetic.
De unde provin aceste informații
- 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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