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Traits
Traits linked to STRADA
STE20 related adaptor alpha
The Human Phenotype Ontology links 49 traits to STRADA, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Big midface | Always |
| Full lower lip | Always |
| Full upper lip | Always |
| Large forehead | Always |
| Long face | Always |
| Wide mouth | Always |
| Wide nasal bridge | Always |
| Abnormal facial shape | Very often (80–99%) |
| Big calvaria | Very often (80–99%) |
| Decreased facial muscle tone | Sometimes (5–29%) |
| Drooling | Sometimes (5–29%) |
| High forehead | Sometimes (5–29%) |
| Highly arched eyebrow | Sometimes (5–29%) |
| Narrow face | Sometimes (5–29%) |
| Open mouth | Sometimes (5–29%) |
| Tented mouth | Sometimes (5–29%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Enlarged brain | Very often (80–99%) |
| Epilepsy | Very often (80–99%) |
| Global developmental delay | Very often (80–99%) |
| Infantile spasms | Very often (80–99%) |
| Cerebral white matter hypoplasia | Often (30–79%) |
| Periventricular white matter hyperintensities | Often (30–79%) |
| Ventriculomegaly | Often (30–79%) |
| Absent speech development | Sometimes (5–29%) |
| Focal impaired awareness seizure | Sometimes (5–29%) |
| Interictal epileptiform activity | Sometimes (5–29%) |
| Repeated seizures without recovery between them | Sometimes (5–29%) |
| Severe global developmental delay | Sometimes (5–29%) |
| Abnormal gait | Not recorded |
| Astrocytosis | Not recorded |
| Inability to walk | Not recorded |
| Intellectual disability | Not recorded |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Low muscle tone | Always |
| Decreased muscle mass | Sometimes (5–29%) |
| Double-Jointed | Sometimes (5–29%) |
| Severely decreased muscle tone | Sometimes (5–29%) |
| Generalized decreased muscle tone | Not recorded |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Abnormal cardiovascular system morphology | Sometimes (5–29%) |
| An opening in the wall separating the top two chambers of the heart | Sometimes (5–29%) |
| Cardiac failure | Sometimes (5–29%) |
Abnormality of prenatal development or birth
| Trait | How often it is seen |
|---|---|
| High levels of amniotic fluid | Always |
| Premature birth | Very often (80–99%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Wide-set eyes | Always |
| Cross-eyed | Not recorded |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Faltering weight | Sometimes (5–29%) |
| Slender build | Not recorded |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Feeding difficulties | Sometimes (5–29%) |
Abnormality of the endocrine system
| Trait | How often it is seen |
|---|---|
| Diabetes insipidus | Sometimes (5–29%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Increased calcium level in kidney | 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 STRADA and how often each is seen. Find out more at hpo.jax.org.
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