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Traits
Traits linked to NAA15
N-alpha-acetyltransferase 15, NatA auxiliary subunit
The Human Phenotype Ontology links 9 traits to NAA15, 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 |
|---|---|
| Intellectual disability | Always |
| Autism spectrum disorder | Very often (80–99%) |
| Motor delay | Very often (80–99%) |
| Delayed speech and language development | Sometimes (5–29%) |
| Epilepsy | Sometimes (5–29%) |
| Attention deficit | Rarely (1–4%) |
| Repetitive movements | Rarely (1–4%) |
| Global developmental delay | Not recorded |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Feeding difficulties | 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 NAA15 and how often each is seen. Find out more at hpo.jax.org.
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