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Traits
Traits linked to TCP1
t-complex 1
The Human Phenotype Ontology links 35 traits to TCP1, 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 |
|---|---|
| Bilateral perisylvian polymicrogyria | Always |
| Delayed speech and language development | Always |
| Focal impaired awareness seizure | Always |
| Grand mal seizures | Always |
| Intellectual disability, mild | Always |
| Interictal epileptiform activity | Always |
| Moderate global developmental delay | Always |
| Multifocal epileptiform discharges | Always |
| Nocturnal seizures | Always |
| Pain insensitivity | Always |
| Periventricular heterotopia | Always |
| Seizure affecting one half of brain | Always |
| Twitching | Always |
| Weakness of one side of body | Always |
| More grooves in brain | Very often (80–99%) |
| Epilepsy | Often (30–79%) |
| Global developmental delay | Often (30–79%) |
| Gray matter heterotopia | Often (30–79%) |
| Hyperintensity of cerebral white matter on MRI | Often (30–79%) |
| Intellectual disability | Often (30–79%) |
| Ventriculomegaly | Often (30–79%) |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Broad opening between the eyelids | Always |
| Dental crowding | Always |
| Fullness around the eyes | Always |
| High palate | Always |
| Highly arched eyebrow | Always |
| Little lower jaw | Always |
| Smooth philtrum | Always |
| Upward slanting of the opening between the eyelids | Always |
| Abnormally small head | Often (30–79%) |
| Big calvaria | Sometimes (5–29%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Jaundice | Always |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Visual impairment | Sometimes (5–29%) |
Abnormality of the immune system
| Trait | How often it is seen |
|---|---|
| Cow milk allergy | Always |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Faltering weight | Always |
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 TCP1 and how often each is seen. Find out more at hpo.jax.org.
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