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Traits
Traits linked to GRB10
growth factor receptor bound protein 10
The Human Phenotype Ontology links 59 traits to GRB10, 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 |
|---|---|
| Little lower jaw | Very often (80–99%) |
| Abnormal facial shape | Often (30–79%) |
| Decreased volume of lip | Often (30–79%) |
| Downturned corners of mouth | Often (30–79%) |
| Prominent forehead | Often (30–79%) |
| Relatively large head | Often (30–79%) |
| Triangular face | Often (30–79%) |
| Decreased size of tooth | Sometimes (5–29%) |
| Deep bite | Sometimes (5–29%) |
| Delayed closure of the soft spot on the skull | Sometimes (5–29%) |
| Dental crowding | Sometimes (5–29%) |
| Frontal bossing | Sometimes (5–29%) |
| High, narrow palate | Sometimes (5–29%) |
| Narrow mouth | Sometimes (5–29%) |
| Pierre-Robin sequence | Sometimes (5–29%) |
| Short chin | Sometimes (5–29%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Delayed speech and language development | Often (30–79%) |
| Global developmental delay | Often (30–79%) |
| Motor delay | Often (30–79%) |
| High pitched voice | Sometimes (5–29%) |
| Obstructive sleep apnea | Sometimes (5–29%) |
| Oral aversion | Sometimes (5–29%) |
| Specific learning disability | Sometimes (5–29%) |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Curvature of digit | Often (30–79%) |
| Short fingers or toes | Often (30–79%) |
| Webbed fingers or toes | Often (30–79%) |
| Curvature of little finger | Sometimes (5–29%) |
| Left and right leg differ in length or width | Sometimes (5–29%) |
| Narrow joint spaces of the elbow | Sometimes (5–29%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Acid reflux | Often (30–79%) |
| Feeding difficulties in infancy | Often (30–79%) |
| Constipation | Sometimes (5–29%) |
| Inflammation of the esophagus | Sometimes (5–29%) |
| Poor appetite | Sometimes (5–29%) |
| Vomiting | Sometimes (5–29%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Growth delay as children | Very often (80–99%) |
| Prenatal growth deficiency | Very often (80–99%) |
| Faltering weight | Often (30–79%) |
| Small for gestational age | Often (30–79%) |
| Uneven or disproportionate growth of one body part compared to another | Often (30–79%) |
| Severe prenatal growth deficiency | Sometimes (5–29%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Abnormality of the genitourinary system | Sometimes (5–29%) |
| Hypospadias | Sometimes (5–29%) |
| Undescended testes | Sometimes (5–29%) |
| Horseshoe kidney | Rarely (1–4%) |
| Renal dysplasia | Rarely (1–4%) |
Abnormality of the endocrine system
| Trait | How often it is seen |
|---|---|
| Decreased response to growth hormone stimulation test | Sometimes (5–29%) |
| Early onset of puberty | Sometimes (5–29%) |
| Premature adrenarche | Sometimes (5–29%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Delayed bone maturation | Very often (80–99%) |
| Decreased muscle mass | Sometimes (5–29%) |
| Scoliosis | Sometimes (5–29%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Excessive sweating | Sometimes (5–29%) |
| Shoulder dimple | Sometimes (5–29%) |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Low blood sugar when fasting | Often (30–79%) |
| Body fails to respond to insulin | Sometimes (5–29%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Abnormality of the heart | Sometimes (5–29%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Abnormality of the outer ear | Often (30–79%) |
Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Aspiration | 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 GRB10 and how often each is seen. Find out more at hpo.jax.org.
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