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Traits
Traits linked to CRAT
carnitine O-acetyltransferase
The Human Phenotype Ontology links 12 traits to CRAT, 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 |
|---|---|
| Ataxia | Always |
| Damage to nerves that sense feeling | Always |
| Degeneration of cerebellum | Always |
| Delayed speech and language development | Always |
| Increased reflexes | Always |
| Iron accumulation in brain | Always |
| Lack of coordination of movement | Always |
| Loss of ability to walk | Always |
| Motor delay | Always |
| Tremor | Always |
| Unsteady walk | Always |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Low muscle tone | 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 CRAT and how often each is seen. Find out more at hpo.jax.org.
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