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Traits
Traits linked to LIN28B
lin-28 RNA binding posttranscriptional regulator B
The Human Phenotype Ontology links 34 traits to LIN28B, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Cancer of early nerve cells | Very often (80–99%) |
| Nervous system cancer | Very often (80–99%) |
| Antalgic gait | Sometimes (5–29%) |
| Irritability | Sometimes (5–29%) |
| Pressure on spinal cord | Sometimes (5–29%) |
| Ataxia | Rarely (1–4%) |
| Jerking | Rarely (1–4%) |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Elevated urinary catecholamines | Very often (80–99%) |
| Fever | Often (30–79%) |
| Elevated serum ferritin | Sometimes (5–29%) |
| Elevated urinary homovanillic acid | Sometimes (5–29%) |
| Elevated urinary vanillylmandelic acid | Sometimes (5–29%) |
| Increased circulating lactate dehydrogenase concentration | Sometimes (5–29%) |
Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Low number of red blood cells or hemoglobin | Often (30–79%) |
| Low platelet count | Often (30–79%) |
| Abnormality of coagulation | Sometimes (5–29%) |
| Bleeding tendency | Sometimes (5–29%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Abdominal bloating | Often (30–79%) |
| Abdominal mass | Often (30–79%) |
| Chronic diarrhea | Often (30–79%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Bulging eye | Sometimes (5–29%) |
| Horner syndrome | Sometimes (5–29%) |
| Opsoclonus | Rarely (1–4%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Swollen lymph nodes | Often (30–79%) |
| High blood pressure | Rarely (1–4%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Anemic pallor | Sometimes (5–29%) |
| Firm lump under the skin | Sometimes (5–29%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Bone pain | Sometimes (5–29%) |
| Spontaneous fracture | Sometimes (5–29%) |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Raccoon eyes | Rarely (1–4%) |
Abnormality of the endocrine system
| Trait | How often it is seen |
|---|---|
| Elevated circulating catecholamine level | Often (30–79%) |
Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Breathing difficulties | Sometimes (5–29%) |
Constitutional symptom
| Trait | How often it is seen |
|---|---|
| Fatigue | Often (30–79%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Weight loss | 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 LIN28B and how often each is seen. Find out more at hpo.jax.org.
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