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Traits
Traits linked to RRAGD
Ras related GTP binding D
The Human Phenotype Ontology links 28 traits to RRAGD, by body system: features seen in people with one of the gene's rare conditions.
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Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Low blood magnesium levels | Always |
| Elevated urine calcium levels | Very often (80–99%) |
| Hypermagnesiuria | Very often (80–99%) |
| Hypokalemic metabolic alkalosis | Very often (80–99%) |
| Low blood calcium levels | Very often (80–99%) |
| Excess fluid in lungs | Often (30–79%) |
| High urine prostaglandin levels | Often (30–79%) |
| Low blood potassium levels | Often (30–79%) |
| Low blood sodium levels | Often (30–79%) |
| Metabolic acidosis | Often (30–79%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Elevated left ventricular end-diastolic diameter | Very often (80–99%) |
| Reduced left ventricular ejection fraction | Very often (80–99%) |
| Stretched and thinned heart muscle | Very often (80–99%) |
| Cardiac failure | Often (30–79%) |
| Fluid around heart | Often (30–79%) |
| Sudden cardiac death | Often (30–79%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Hyperactive movements | Often (30–79%) |
| Hypocalcemic tetany | Often (30–79%) |
| Myoclonic spasms | Often (30–79%) |
| Epilepsy | Sometimes (5–29%) |
| Grand mal seizures | Sometimes (5–29%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Abnormal renal tubular resorption | Often (30–79%) |
| Increased calcium level in kidney | Often (30–79%) |
| Increased urine output | Often (30–79%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Hepatic calcification | Often (30–79%) |
Abnormality of the endocrine system
| Trait | How often it is seen |
|---|---|
| Elevated plasma aldosterone | Often (30–79%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Intermittent involuntary muscle spasm | Often (30–79%) |
Constitutional symptom
| Trait | How often it is seen |
|---|---|
| Joint 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 RRAGD and how often each is seen. Find out more at hpo.jax.org.
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