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Traits
Traits linked to CLPX
caseinolytic mitochondrial matrix peptidase chaperone subunit X
The Human Phenotype Ontology links 3 traits to CLPX, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Iron deficiency anemia | Often (30–79%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Photosensitive skin | Always |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Increased erythrocyte protoporphyrin concentration | 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 CLPX and how often each is seen. Find out more at hpo.jax.org.
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