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Traits
Traits linked to WNT9B
Wnt family member 9B
The Human Phenotype Ontology links 18 traits to WNT9B, 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 |
|---|---|
| Eye folds | Very often (80–99%) |
| Flat nose | Very often (80–99%) |
| Cleft palate | Sometimes (5–29%) |
| Non-midline cleft of the upper lip | Sometimes (5–29%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Absent kidney | Very often (80–99%) |
| Urogenital fistula | Often (30–79%) |
| Abnormal morphology of female internal genitalia | Sometimes (5–29%) |
Abnormality of prenatal development or birth
| Trait | How often it is seen |
|---|---|
| Low levels of amniotic fluid | Very often (80–99%) |
| Fetal polyuria | Often (30–79%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Abnormal connection between trachea and esophagus | Often (30–79%) |
| Abnormality of the intestine | Often (30–79%) |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Sirenomelia | Sometimes (5–29%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Abnormal cardiovascular system morphology | Often (30–79%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Low-set ears | Very often (80–99%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Wide-set eyes | Very often (80–99%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Abnormal sacrum morphology | Often (30–79%) |
Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Poorly developed lungs | Very often (80–99%) |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Nonketotic hypoglycemia | 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 WNT9B and how often each is seen. Find out more at hpo.jax.org.
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