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Traits
Traits linked to IL1RN
interleukin 1 receptor antagonist
The Human Phenotype Ontology links 27 traits to IL1RN, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Broad ribs | Always |
| Flaring of rib cage | Always |
| Osteopenia | Always |
| Breakdown of bone | Very often (80–99%) |
| Fused neck | Often (30–79%) |
| Periostitis | Not recorded |
Abnormality of the immune system
| Trait | How often it is seen |
|---|---|
| Abscess | Always |
| Bone infection | Always |
| Pimple | Always |
| Skin rash | Always |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Elevated circulating C-reactive protein concentration | Always |
| High ESR | Always |
| Joint swelling | Always |
| Increased level of L-fucose in urine | Not recorded |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Enlarged liver | Not recorded |
| Stomach cancer | Not recorded |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Hyperkeratosis | Always |
| Thickening of upper layer of skin | Always |
Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Pulmonary scarring | Sometimes (5–29%) |
| Breathing difficulties | Not recorded |
Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Increased blood neutrophil counts | Always |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Inflammation of the mouth | Not recorded |
Abnormality of prenatal development or birth
| Trait | How often it is seen |
|---|---|
| Fetal distress | Often (30–79%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Increased spleen size | Not recorded |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Motor delay | Always |
Constitutional symptom
| Trait | How often it is seen |
|---|---|
| Joint pain | Not recorded |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Faltering weight in infancy | 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 IL1RN and how often each is seen. Find out more at hpo.jax.org.
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