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Traits
Traits linked to NRAP
nebulin related anchoring protein
The Human Phenotype Ontology links 40 traits to NRAP, 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 |
|---|---|
| Aborted sudden cardiac death | Always |
| Cardiac failure | Always |
| Decreased cardiac output | Always |
| Elevated left ventricular end-diastolic diameter | Always |
| Enlarged heart | Always |
| Heart stops beating | Always |
| High blood pressure | Always |
| Increased left ventricular end-diastolic volume | Always |
| Inflammation of heart muscle | Always |
| Left atrial enlargement | Always |
| Left bundle branch block | Always |
| Left ventricular dilatation | Always |
| Left ventricular noncompaction | Always |
| Low-output congestive heart failure | Always |
| Mitral regurgitation | Always |
| Myocardial late gadolinium enhancement | Always |
| Prolonged QTc interval | Always |
| Right ventricular dilatation | Always |
| Sinus tachycardia | Always |
| Stretched and thinned heart muscle | Always |
| Systolic heart murmur | Always |
| Tricuspid regurgitation | Always |
| Ventricular tachycardia | Always |
| Left ventricular systolic dysfunction | Very often (80–99%) |
| Abnormal heart rate | Often (30–79%) |
| Moderately reduced left ventricular ejection fraction | Often (30–79%) |
| Severely reduced left ventricular ejection fraction | Often (30–79%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Low muscle tone | Always |
| EMG abnormality | Sometimes (5–29%) |
| Loss of fat tissue in localized area | Sometimes (5–29%) |
| Muscle tissue disease | Sometimes (5–29%) |
Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Orthopnea | Always |
| Respiratory tract infection | Always |
| Exertional breathlessness | Often (30–79%) |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Elevated circulating NT-proBNP concentration | Always |
| Fluid retention | Often (30–79%) |
Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Thromboembolic stroke | Sometimes (5–29%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Sensorineural hearing impairment | Sometimes (5–29%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Motor delay | Always |
Constitutional symptom
| Trait | How often it is seen |
|---|---|
| Fatigue | 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 NRAP and how often each is seen. Find out more at hpo.jax.org.
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