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Traits
Traits linked to CR2
complement C3d receptor 2
The Human Phenotype Ontology links 75 traits to CR2, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the immune system
Abnormal cellular phenotype
| Trait | How often it is seen |
|---|---|
| Chronic absent circulating IgG4 | Always |
| Chronic decreased circulating IgG1 concentration | Always |
| Decreased circulating IgA concentration | Always |
| Decreased circulating total IgG concentration | Always |
| Decreased circulating IgG concentration | Very often (80–99%) |
| Impaired T cell function | Not recorded |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Recurrent sinus disease | Always |
| Abnormal color of the oral mucosa | Sometimes (5–29%) |
| Abnormality of salivation | Sometimes (5–29%) |
| Inflammation of the lips | Sometimes (5–29%) |
| Mouth sore | Sometimes (5–29%) |
| Pink eye | Not recorded |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Increased spleen size | Always |
| High blood pressure | Often (30–79%) |
| Raynaud phenomenon | Often (30–79%) |
| Swollen lymph nodes | Sometimes (5–29%) |
| Follicular hyperplasia | Not recorded |
Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Decreased blood leukocyte number | Often (30–79%) |
| Hemolytic anemia | Sometimes (5–29%) |
| Low platelet count | Sometimes (5–29%) |
| Cancer of lymphatic system | Not recorded |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Chronic diarrhea | Always |
| Anorexia | Very often (80–99%) |
| Diarrhea | Not recorded |
| Enlarged liver | Not recorded |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Fever | Always |
| High urine protein levels | Very often (80–99%) |
| Blood in urine | Often (30–79%) |
| High urine neutrophil count | Often (30–79%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Depression | Sometimes (5–29%) |
| Epilepsy | Sometimes (5–29%) |
| Chorea | Rarely (1–4%) |
Constitutional symptom
| Trait | How often it is seen |
|---|---|
| Muscle ache | Always |
| Fatigue | Very often (80–99%) |
| Malaise | Very often (80–99%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Frequent urinary tract infections | Always |
| Lupus nephritis | Often (30–79%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Hair loss | Often (30–79%) |
| Photosensitive skin | Sometimes (5–29%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Arthritis | Often (30–79%) |
| Polyarticular arthritis | Often (30–79%) |
Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Sore throat | Always |
| Permanent enlargement of the airways of the lungs | Not recorded |
Abnormal tissue mass
| Trait | How often it is seen |
|---|---|
| Abnormal tissue mass | Not recorded |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Recurrent middle ear infection | Always |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Noninflammatory retina disease | Rarely (1–4%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Weight loss | Very often (80–99%) |
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 CR2 and how often each is seen. Find out more at hpo.jax.org.
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