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Traits
Traits linked to LMOD2
leiomodin 2
The Human Phenotype Ontology links 28 traits to LMOD2, 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 |
|---|---|
| Aortic regurgitation | Always |
| Complete right bundle branch block | Always |
| Elevated heart rate | Always |
| Left atrial enlargement | Always |
| Mitral regurgitation | Always |
| Monomorphic ventricular tachycardia | Always |
| Myofiber disarray | Always |
| Paroxysmal ventricular tachycardia | Always |
| Severely reduced left ventricular ejection fraction | Always |
| Stretched and thinned heart muscle | Always |
| Left ventricular systolic dysfunction | Very often (80–99%) |
| Abnormal heart rate | Often (30–79%) |
| Cardiac failure | Often (30–79%) |
| Cardiogenic shock | Often (30–79%) |
| Multifocal atrial tachycardia | Often (30–79%) |
| Tricuspid regurgitation | Often (30–79%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Increased Z-disc width | Often (30–79%) |
| EMG abnormality | Sometimes (5–29%) |
| Loss of fat tissue in localized area | Sometimes (5–29%) |
| Muscle tissue disease | Sometimes (5–29%) |
Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Bleeding in brain | Always |
| Thromboembolic stroke | Sometimes (5–29%) |
Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Exertional breathlessness | Often (30–79%) |
| Orthopnea | Often (30–79%) |
Abnormal cellular phenotype
| Trait | How often it is seen |
|---|---|
| Myocardial sarcomeric disarray | Often (30–79%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Sensorineural hearing impairment | Sometimes (5–29%) |
Constitutional symptom
| Trait | How often it is seen |
|---|---|
| Fatigue | Often (30–79%) |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Fluid retention | 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 LMOD2 and how often each is seen. Find out more at hpo.jax.org.
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