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Traits
Traits linked to ZNF668
zinc finger protein 668
The Human Phenotype Ontology links 28 traits to ZNF668, 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 |
|---|---|
| Abnormally small head | Always |
| Prominent nose | Always |
| Big maxilla | Often (30–79%) |
| High palate | Often (30–79%) |
| Little lower jaw | Often (30–79%) |
| Skin tag in front of the ear | Often (30–79%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Global developmental delay | Always |
| Intellectual disability | Always |
| Brain degeneration | Often (30–79%) |
| Epilepsy | Often (30–79%) |
| Epileptic encephalopathy | Often (30–79%) |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Long big toe | Always |
| Broad thumb | Often (30–79%) |
| Bunion | Often (30–79%) |
| Curvature of digit | Often (30–79%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Low muscle tone | Always |
| Lower limb spasticity | Often (30–79%) |
| Osteopenia | Often (30–79%) |
| Pigeon chest | Often (30–79%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Birth defect that causes a hole in the innermost layer at the back of the eye | Often (30–79%) |
| Deeply set eye | Often (30–79%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Faltering weight | Always |
| Small for gestational age | Always |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Secundum atrial septal defect | Often (30–79%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Feeding difficulties | Often (30–79%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Large ears | Always |
Abnormality of the immune system
| Trait | How often it is seen |
|---|---|
| Recurrent chest infections | Often (30–79%) |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Diabetes mellitus | 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 ZNF668 and how often each is seen. Find out more at hpo.jax.org.
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