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Traits
Traits linked to FGD4
FYVE, RhoGEF and PH domain containing 4
The Human Phenotype Ontology links 19 traits to FGD4, 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 |
|---|---|
| Absent reflexes | Always |
| Decreased motor nerve conduction velocity | Always |
| Decreased number of peripheral myelinated nerve fibers | Always |
| Motor delay | Always |
| Numbness | Always |
| Onion bulb formation | Always |
| Unsteady walk | Always |
| Decreased reflex response | Not recorded |
| Decreased sensation in extremities | Not recorded |
| Peripheral hypomyelination | Not recorded |
| Waddling gait | Not recorded |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Club feet | Often (30–79%) |
| Small hypothenar eminence | Often (30–79%) |
| Small thenar eminence | Often (30–79%) |
| Decreased arm strength | Not recorded |
| Distal lower limb muscle weakness | Not recorded |
| High-arched foot | Not recorded |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Scoliosis | Often (30–79%) |
| Distal lower limb amyotrophy | 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 FGD4 and how often each is seen. Find out more at hpo.jax.org.
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