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Traits
Traits linked to SCN10A
sodium voltage-gated channel alpha subunit 10
The Human Phenotype Ontology links 28 traits to SCN10A, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Redness of skin or mucous membrane | Very often (80–99%) |
| Complete right bundle branch block | Often (30–79%) |
| Fainting spell | Often (30–79%) |
| Heart stops beating | Often (30–79%) |
| ST segment elevation | Often (30–79%) |
| Elevated heart rate | Sometimes (5–29%) |
| First degree atrioventricular block | Sometimes (5–29%) |
| Inflammation of blood vessel | Sometimes (5–29%) |
| Paroxysmal ventricular tachycardia | Sometimes (5–29%) |
| Sick sinus syndrome | Sometimes (5–29%) |
| Supraventricular tachycardia | Sometimes (5–29%) |
| Ventricular fibrillation | Sometimes (5–29%) |
| Trifascicular block | Rarely (1–4%) |
| Ventricular arrhythmia | Rarely (1–4%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Dysesthesia | Always |
| Epilepsy | Very often (80–99%) |
| Peripheral neuropathy | Very often (80–99%) |
| Decreased sensation in extremities | Sometimes (5–29%) |
Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Blood cancer | Sometimes (5–29%) |
| Platelet abnormalities | Sometimes (5–29%) |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Decreased/absent ankle reflexes | Sometimes (5–29%) |
| Fluid accumulation in lower limbs | Sometimes (5–29%) |
Constitutional symptom
| Trait | How often it is seen |
|---|---|
| Erythromelalgia | Very often (80–99%) |
| Allodynia | Sometimes (5–29%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Constipation | Often (30–79%) |
Abnormality of the immune system
| Trait | How often it is seen |
|---|---|
| Recurrent respiratory infections | Sometimes (5–29%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Itching | Often (30–79%) |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Hypothermia | Sometimes (5–29%) |
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 SCN10A and how often each is seen. Find out more at hpo.jax.org.
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