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Traits
Traits linked to CORIN
corin, serine peptidase
The Human Phenotype Ontology links 33 traits to CORIN, 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 |
|---|---|
| High blood pressure | Always |
| Left atrial enlargement | Always |
| Left atrial fibrosis | Always |
| Elevated diastolic blood pressure | Very often (80–99%) |
| Elevated systolic blood pressure | Very often (80–99%) |
| Atrial flutter | Often (30–79%) |
| Quivering upper heart chambers resulting in irregular heartbeat | Often (30–79%) |
| Abnormality of liver blood vessels | Sometimes (5–29%) |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Decreased circulating NT-proANP concentration | Always |
| Increased circulating brain natriuretic peptide concentration | Always |
| High urine protein levels | Very often (80–99%) |
| Excess fluid in lungs | Often (30–79%) |
| High liver enzymes | Sometimes (5–29%) |
| Elevated creatinine | Rarely (1–4%) |
| Type 1 diabetes | Rarely (1–4%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Renal failure | Often (30–79%) |
| Abnormality of the kidney | Sometimes (5–29%) |
| Acute kidney injury | Rarely (1–4%) |
| Chronic kidney disease | Rarely (1–4%) |
| Polycystic ovaries | Rarely (1–4%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Abnormality of the nervous system | Sometimes (5–29%) |
| Headache | Sometimes (5–29%) |
| Difficulty sleeping | Rarely (1–4%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Increased body mass index | Sometimes (5–29%) |
| Prenatal growth deficiency | Sometimes (5–29%) |
| Small for gestational age | Sometimes (5–29%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Abdominal pain | Sometimes (5–29%) |
| Helicobacter pylori infection | Rarely (1–4%) |
Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Low platelet count | Rarely (1–4%) |
Abnormality of prenatal development or birth
| Trait | How often it is seen |
|---|---|
| Placental issue | Very often (80–99%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Abnormality of vision | Sometimes (5–29%) |
Abnormality of the immune system
| Trait | How often it is seen |
|---|---|
| Autoimmunity | Rarely (1–4%) |
Constitutional symptom
| Trait | How often it is seen |
|---|---|
| Epigastric pain | 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 CORIN and how often each is seen. Find out more at hpo.jax.org.
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