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Traits
Traits linked to INTS11
integrator complex subunit 11
The Human Phenotype Ontology links 42 traits to INTS11, 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 |
|---|---|
| Agenesis of corpus callosum | Always |
| Brain degeneration | Always |
| Degeneration of cerebellum | Always |
| Degeneration of cerebrum | Always |
| Delayed CNS myelination | Always |
| Delayed speech and language development | Always |
| Dilated fourth ventricle | Always |
| Epilepsy | Always |
| Hyperintensity of cerebral white matter on MRI | Always |
| Intellectual disability, mild | Always |
| Intellectual disability, severe | Always |
| Leukoencephalopathy | Always |
| Motor delay | Always |
| Pontocerebellar atrophy | Always |
| Severe global developmental delay | Always |
| Simplified gyral pattern | Always |
| Small cerebellum | Always |
| Ventriculomegaly | Always |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Abnormally small head | Always |
| Bifid uvula | Always |
| Coarse facial features | Always |
| Deformity of the skull | Always |
| Eye folds | Always |
| Narrow palate | Always |
| Prominent area between the eyebrows | Always |
| Receding chin | Always |
| Sloping forehead | Always |
| Small forehead | Always |
| Thin red part of the upper lip | Always |
| Triangular face | Always |
| Wide mouth | Always |
| Wide nose | Always |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Astigmatism | Always |
| Breakdown of light-sensitive cells in back of eye | Always |
| Close sighted | Always |
| Cross-eyed | Always |
| Optic atrophy | Always |
| Wide-set eyes | Always |
Abnormality of prenatal development or birth
| Trait | How often it is seen |
|---|---|
| Premature birth | Always |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Low-set ears | Always |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Low muscle tone | Always |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Prenatal growth deficiency | 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 INTS11 and how often each is seen. Find out more at hpo.jax.org.
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