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Traits
Traits linked to PIGF
phosphatidylinositol glycan anchor biosynthesis class F
The Human Phenotype Ontology links 26 traits to PIGF, 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 |
|---|---|
| Abnormally small head | Often (30–79%) |
| Coarse facial features | Often (30–79%) |
| Decreased size of tooth | Often (30–79%) |
| Delayed eruption of permanent teeth | Often (30–79%) |
| Little lower jaw | Often (30–79%) |
| Narrow mouth | Often (30–79%) |
| Nasal tip, upturned | Often (30–79%) |
| Open mouth | Often (30–79%) |
| Short nose | Often (30–79%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Small thumbnail | Always |
| Underdeveloped fifth fingernail | Always |
| Underdeveloped toenails | Always |
| Absent fifth toenail | Often (30–79%) |
| Small fingernail | Often (30–79%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Global developmental delay | Always |
| Intellectual disability, severe | Always |
| Absent speech development | Often (30–79%) |
| Grand mal seizures | Often (30–79%) |
| Head-banging | Often (30–79%) |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Bilateral triphalangeal thumbs | Often (30–79%) |
| Short outermost bone of toe | Often (30–79%) |
| Short outermost finger bone | Often (30–79%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| An opening in the wall separating the top two chambers of the heart | Often (30–79%) |
Abnormality of the endocrine system
| Trait | How often it is seen |
|---|---|
| Early onset of puberty | Often (30–79%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Poor head control | Often (30–79%) |
Constitutional symptom
| Trait | How often it is seen |
|---|---|
| Impaired toileting ability | 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 PIGF and how often each is seen. Find out more at hpo.jax.org.
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