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Traits
Traits linked to CRBN
cereblon
The Human Phenotype Ontology links 8 traits to CRBN, 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, mild | Always |
| Intellectual disability, severe | Always |
| Self-injurious behavior | Always |
| Epilepsy | Very often (80–99%) |
| Attention deficit | Often (30–79%) |
| Delayed ability to walk | Often (30–79%) |
| Absent speech development | Sometimes (5–29%) |
| Global developmental delay | Not recorded |
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 CRBN and how often each is seen. Find out more at hpo.jax.org.
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