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Traits
Traits linked to ITGAM
integrin subunit alpha M
The Human Phenotype Ontology links 44 traits to ITGAM, 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 |
|---|---|
| Antinuclear antibody positivity | Very often (80–99%) |
| Anti-complement component C1q antibody positivity | Often (30–79%) |
| Anti-ribosome Po antibody positivity | Often (30–79%) |
| Anti-titin antibody positivity | Often (30–79%) |
| Antineutrophil antibody positivity | Often (30–79%) |
| Decreased circulating complement C3 concentration | Often (30–79%) |
| Decreased circulating complement C4 concentration | Often (30–79%) |
| Malar rash | Often (30–79%) |
| Anti-dsDNA antibody positivity | Sometimes (5–29%) |
| Anti-La/SS-B antibody positivity | Sometimes (5–29%) |
| Anti-nucleoporin 62 antibody positivity | Sometimes (5–29%) |
| Anti-phosphatidic acid antibody positivity | Sometimes (5–29%) |
| Anti-Ro52/TRIM21 antibody positivity | Sometimes (5–29%) |
| Anti-Sm antibody positivity | Sometimes (5–29%) |
| Anti-U1 ribonucleoprotein antibody positivity | Sometimes (5–29%) |
| Discoid lupus rash | Sometimes (5–29%) |
| Serositis | Sometimes (5–29%) |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| 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%) |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Fever | Very often (80–99%) |
| High urine protein levels | Very often (80–99%) |
| Blood in urine | Often (30–79%) |
| High urine neutrophil count | Often (30–79%) |
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%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| High blood pressure | Often (30–79%) |
| Raynaud phenomenon | Often (30–79%) |
| Swollen lymph nodes | Sometimes (5–29%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Depression | Sometimes (5–29%) |
| Epilepsy | Sometimes (5–29%) |
| Chorea | Rarely (1–4%) |
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%) |
Constitutional symptom
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Anorexia | Very often (80–99%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Noninflammatory retina disease | Rarely (1–4%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Lupus nephritis | Often (30–79%) |
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 ITGAM and how often each is seen. Find out more at hpo.jax.org.
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