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Traits
Traits linked to HBA2
hemoglobin subunit alpha 2
The Human Phenotype Ontology links 52 traits to HBA2, 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
| Trait | How often it is seen |
|---|---|
| Abnormal hemoglobin | Very often (80–99%) |
| HbH hemoglobin | Very often (80–99%) |
| Low number of red blood cells or hemoglobin | Very often (80–99%) |
| Microcytic anemia | Very often (80–99%) |
| Bruising susceptibility | Often (30–79%) |
| Heinz bodies | Not recorded |
| Heinz body anemia | Not recorded |
| Hemolytic anemia | Not recorded |
| Hypochromic microcytic anemia | Not recorded |
| Increased circulating hemoglobin concentration | Not recorded |
| Increased hematocrit | Not recorded |
| Increased red blood cells | Not recorded |
| Nonspherocytic hemolytic anemia | Not recorded |
| Reduced alpha/beta synthesis ratio | Not recorded |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Abnormally small head | Often (30–79%) |
| Broad forehead | Often (30–79%) |
| Downward slanting of the opening between the eyelids | Often (30–79%) |
| Eye folds | Often (30–79%) |
| High forehead | Often (30–79%) |
| High palate | Often (30–79%) |
| Little lower jaw | Often (30–79%) |
| Receding chin | Often (30–79%) |
| Short neck | Often (30–79%) |
| Wide nasal bridge | Often (30–79%) |
| Zygomatic flattening | Often (30–79%) |
| Flattened bony protrusion above eyes | Sometimes (5–29%) |
| Frontal bossing | Sometimes (5–29%) |
| Sparse or absent eyebrows | Sometimes (5–29%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Cardiac failure | Very often (80–99%) |
| Increased spleen size | Often (30–79%) |
| Swelling or irritation of membrane around heart | Sometimes (5–29%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Low muscle tone | Often (30–79%) |
| Pigeon chest | Often (30–79%) |
| Flexed joint that cannot be straightened | Sometimes (5–29%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Abnormal speech pattern | Very often (80–99%) |
| Intellectual disability | Very often (80–99%) |
| Too much cerebrospinal fluid in the brain | Often (30–79%) |
Abnormality of limbs
Abnormality of prenatal development or birth
| Trait | How often it is seen |
|---|---|
| High levels of amniotic fluid | Often (30–79%) |
| Low levels of amniotic fluid | Often (30–79%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Absent/small ear lobes | Often (30–79%) |
| Ears rotated toward back of head | Often (30–79%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Undescended testes | Often (30–79%) |
| Hypospadias | Sometimes (5–29%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Faltering weight | Often (30–79%) |
| Short stature | Often (30–79%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Enlarged liver | Often (30–79%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Wide-set eyes | Often (30–79%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Paleness | Very often (80–99%) |
Constitutional symptom
| Trait | How often it is seen |
|---|---|
| Fatigue | Very often (80–99%) |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Hydrops fetalis | Very often (80–99%) |
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 HBA2 and how often each is seen. Find out more at hpo.jax.org.
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