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Traits
Traits linked to IGHM
immunoglobulin heavy constant mu
The Human Phenotype Ontology links 39 traits to IGHM, 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%) |
| Recurrent enteroviral infections | Often (30–79%) |
| Recurrent pneumonia | Often (30–79%) |
| Infection in blood stream | Sometimes (5–29%) |
| Meningitis | Sometimes (5–29%) |
| Recurrent bacterial infections | 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%) |
| Recurrent sinus disease | Sometimes (5–29%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Diarrhea | Very often (80–99%) |
| Chronic diarrhea | Sometimes (5–29%) |
| Liver inflammation | Sometimes (5–29%) |
| Malabsorption | Sometimes (5–29%) |
| Rectal abscess | Sometimes (5–29%) |
Abnormal cellular phenotype
| Trait | How often it is seen |
|---|---|
| Decreased circulating antibody level | Always |
| Panhypogammaglobulinemia | Always |
| Agammaglobulinemia | Very often (80–99%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Chronic infections of the middle ear | Very often (80–99%) |
| Abnormally shaped ears | Sometimes (5–29%) |
| Recurrent middle ear infection | Sometimes (5–29%) |
Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Low B cell count | Always |
| Low blood neutrophil count | Often (30–79%) |
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 IGHM and how often each is seen. Find out more at hpo.jax.org.
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