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Traits
Traits linked to NUDT2
nudix hydrolase 2
The Human Phenotype Ontology links 16 traits to NUDT2, 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 ability to walk | Always |
| Delayed speech and language development | Always |
| Eye of the tiger anomaly of globus pallidus | Always |
| Global developmental delay | Always |
| Intellectual disability, borderline | Always |
| Motor delay | Always |
| Thin corpus callosum | Always |
| Unsteady walk | Always |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Low frontal hairline | Always |
| Monobrow | Always |
| Receding chin | Always |
| Wide nasal bridge | Always |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Frequent falls | Always |
| Low muscle tone | Always |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Poor suck | Always |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Small for gestational age | 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 NUDT2 and how often each is seen. Find out more at hpo.jax.org.
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