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Traits
Traits linked to GP1BA
glycoprotein Ib platelet subunit alpha
The Human Phenotype Ontology links 45 traits to GP1BA, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of blood and blood-forming tissues
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Abnormality of the nervous system | Rarely (1–4%) |
| Cerebral palsy | Rarely (1–4%) |
| Epilepsy | Rarely (1–4%) |
| Global developmental delay | Rarely (1–4%) |
| Migraine | Rarely (1–4%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Blindness | Rarely (1–4%) |
| Nonarteritic anterior ischemic optic neuropathy | Not recorded |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Blood in urine | Sometimes (5–29%) |
| Bloody urine | Sometimes (5–29%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Increased spleen size | Not recorded |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Partially duplicated kidney | Rarely (1–4%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Bilateral sensorineural hearing impairment | Rarely (1–4%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Abnormal uterus bleeding | Sometimes (5–29%) |
Abnormality of the immune system
| Trait | How often it is seen |
|---|---|
| Asthma | Rarely (1–4%) |
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 GP1BA and how often each is seen. Find out more at hpo.jax.org.
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