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Traits
Traits linked to TET3
tet methylcytosine dioxygenase 3
The Human Phenotype Ontology links 38 traits to TET3, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Delayed motor skills | Always |
| Delayed speech and language development | Always |
| Global developmental delay | Always |
| Poor social interactions | Always |
| Autism spectrum disorder | Very often (80–99%) |
| Delayed fine motor development | Very often (80–99%) |
| Intellectual disability | Very often (80–99%) |
| Anxiety | Often (30–79%) |
| Attention deficit | Often (30–79%) |
| EEG abnormality | Often (30–79%) |
| Epilepsy | Often (30–79%) |
| Depression | Sometimes (5–29%) |
| Extra-axial cerebrospinal fluid accumulation | Sometimes (5–29%) |
| Periventricular leukomalacia | Sometimes (5–29%) |
| Ventriculomegaly | Sometimes (5–29%) |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Broad head shape | Often (30–79%) |
| Decreased facial muscle tone | Often (30–79%) |
| High palate | Often (30–79%) |
| Long face | Often (30–79%) |
| Long philtrum | Often (30–79%) |
| Open mouth | Often (30–79%) |
| Abnormally small head | Sometimes (5–29%) |
| Big calvaria | Sometimes (5–29%) |
| Narrowing of the tear duct | Sometimes (5–29%) |
| Broad forehead | Not recorded |
| High forehead | Not recorded |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Generalized decreased muscle tone | Often (30–79%) |
| Abnormal formation of the hip | Sometimes (5–29%) |
| Advanced bone age | Sometimes (5–29%) |
| Double-Jointed | Sometimes (5–29%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Cross-eyed | Sometimes (5–29%) |
| Drooping upper eyelid | Sometimes (5–29%) |
| Involuntary, rapid, rhythmic eye movements | Sometimes (5–29%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Enlarged heart | Sometimes (5–29%) |
| Hole in heart wall separating two lower heart chambers | Sometimes (5–29%) |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Dropped arches | Sometimes (5–29%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Feeding difficulties in infancy | Often (30–79%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Prominent ear | 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 TET3 and how often each is seen. Find out more at hpo.jax.org.
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