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Traits
Traits linked to IGLL1
immunoglobulin lambda like polypeptide 1
The Human Phenotype Ontology links 35 traits to IGLL1, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the immune system
| Trait | How often it is seen |
|---|---|
| Decreased immune function | Very often (80–99%) |
| Recurrent infections | Very often (80–99%) |
| Recurrent respiratory infections | Very often (80–99%) |
| Recurrent skin infections | Very often (80–99%) |
| Skin rash | Very often (80–99%) |
| Bone infection | Often (30–79%) |
| Infection in blood stream | Sometimes (5–29%) |
| Meningitis | Sometimes (5–29%) |
| Recurrent bacterial infections | Not recorded |
| Recurrent pneumonia | Not recorded |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Pink eye | Very often (80–99%) |
| Sinus disease | Very often (80–99%) |
| Eye folds | Sometimes (5–29%) |
| High palate | Sometimes (5–29%) |
Abnormal cellular phenotype
| Trait | How often it is seen |
|---|---|
| Decreased circulating IgA concentration | Always |
| Decreased circulating IgM concentration | Always |
| Agammaglobulinemia | Very often (80–99%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Diarrhea | Very often (80–99%) |
| Liver inflammation | Sometimes (5–29%) |
| Malabsorption | Sometimes (5–29%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Recurrent middle ear infection | Always |
| Chronic infections of the middle ear | Very often (80–99%) |
| Abnormally shaped ears | Sometimes (5–29%) |
Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Absent circulating B cells | Always |
| Low blood neutrophil count | Sometimes (5–29%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Arthritis | Often (30–79%) |
| Bacterial infection of skin | Sometimes (5–29%) |
Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Cough | Very often (80–99%) |
| Permanent enlargement of the airways of the lungs | Sometimes (5–29%) |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Fever | Very often (80–99%) |
| Dehydration | Sometimes (5–29%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Wide-set eyes | Sometimes (5–29%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Warts | Sometimes (5–29%) |
Constitutional symptom
| Trait | How often it is seen |
|---|---|
| Fatigue | Very often (80–99%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Faltering weight | 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 IGLL1 and how often each is seen. Find out more at hpo.jax.org.
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