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Traits
Traits linked to TRIM37
tripartite motif containing 37
The Human Phenotype Ontology links 44 traits to TRIM37, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Big calvaria | Very often (80–99%) |
| Depressed nasal bridge | Very often (80–99%) |
| Frontal bossing | Very often (80–99%) |
| J-shaped sella turcica | Very often (80–99%) |
| Triangular face | Very often (80–99%) |
| Wide nose | Very often (80–99%) |
| Absent frontal sinuses | Often (30–79%) |
| Bad bite | Often (30–79%) |
| Wide nasal bridge | Often (30–79%) |
| Thin dental enamel | Rarely (1–4%) |
| Abnormally small tongue | Not recorded |
| Dental crowding | Not recorded |
| Failure of development of between one and six teeth | Not recorded |
| Hypoplastic frontal sinuses | Not recorded |
| Long, narrow head | Not recorded |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Corneal dystrophy | Sometimes (5–29%) |
| Cross-eyed | Sometimes (5–29%) |
| Cat eye | Rarely (1–4%) |
| Astigmatism | Not recorded |
| Pigmentary retinopathy | Not recorded |
| Wide-set eyes | Not recorded |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Diminished deep tendon reflex | Very often (80–99%) |
| High pitched voice | Very often (80–99%) |
| Intellectual disability, mild | Sometimes (5–29%) |
| Ventriculomegaly | Sometimes (5–29%) |
| Difficulty articulating speech | Not recorded |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Pericardial constriction | Often (30–79%) |
| Enlarged heart | Sometimes (5–29%) |
| Cardiac failure | Not recorded |
| Myocardial fibrosis | Not recorded |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Growth delay | Very often (80–99%) |
| Prenatal growth deficiency | Very often (80–99%) |
| Short stature | Very often (80–99%) |
| Wasting syndrome | Very often (80–99%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Enlarged liver | Very often (80–99%) |
| Accumulation of fluid in the abdomen | Sometimes (5–29%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Low muscle tone | Often (30–79%) |
| Thickened cortex of long bones | Sometimes (5–29%) |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Single transverse palmar crease | Rarely (1–4%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Nephroblastoma | Sometimes (5–29%) |
Abnormality of the immune system
| Trait | How often it is seen |
|---|---|
| Recurrent chest infections | Often (30–79%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| port-wine stain | Often (30–79%) |
Abnormality of the voice
| Trait | How often it is seen |
|---|---|
| Weak voice | Very often (80–99%) |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Hydrops fetalis | Rarely (1–4%) |
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 TRIM37 and how often each is seen. Find out more at hpo.jax.org.
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