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Traits
Traits linked to IFT81
intraflagellar transport 81
The Human Phenotype Ontology links 27 traits to IFT81, 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 |
|---|---|
| Long, narrow head | Always |
| Prominent back of the head | Always |
| Relatively large head | Always |
| Long philtrum | Often (30–79%) |
| Midface retrusion | Often (30–79%) |
| Depressed nasal bridge | Not recorded |
| Prominent forehead | Not recorded |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Generalized decreased muscle tone | Always |
| Short ribs | Often (30–79%) |
| Hook-shaped collarbone | Not recorded |
| Horizontal ribs | Not recorded |
| Narrow chest | Not recorded |
| Small chest | Not recorded |
| Small wings of the pelvic girdle | Not recorded |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Postaxial polydactyly | Often (30–79%) |
| Smaller or shorter than typical limbs | Often (30–79%) |
| Short fingers or toes | Not recorded |
| Underdeveloped outer large forearm bone | Not recorded |
| Webbed fingers or toes | Not recorded |
Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Breathing difficulties | Not recorded |
| Poorly developed lungs | Not recorded |
| Respiratory failure | Not recorded |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Hole in heart wall separating two lower heart chambers | Often (30–79%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Omphalocele | Not recorded |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Low-set ears | Often (30–79%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Bulging eye | Not recorded |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Ambiguous external genitalia | Not recorded |
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 IFT81 and how often each is seen. Find out more at hpo.jax.org.
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