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Traits
Traits linked to CENPF
centromere protein F
The Human Phenotype Ontology links 30 traits to CENPF, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Abnormally small eyeball | Not recorded |
| Cat eye | Not recorded |
| Clouding of the lens of the eye | Not recorded |
| Cornea of eye less than 10mm in diameter | Not recorded |
| Deeply set eye | Not recorded |
| Hardening of skin and connective tissue | Not recorded |
| Optic nerve hypoplasia | Not recorded |
| Peters anomaly | Not recorded |
| Wide-set eyes | Not recorded |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Abnormally small head | Not recorded |
| Cleft palate | Not recorded |
| Little lower jaw | Not recorded |
| Prominent nasal bridge | Not recorded |
| Short columella | Not recorded |
| Wide mouth | Not recorded |
| Wide nasal bridge | Not recorded |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Agenesis of corpus callosum | Not recorded |
| Cerebellar vermis hypoplasia | Not recorded |
| Small cerebellum | Not recorded |
| Too much cerebrospinal fluid in the brain | Not recorded |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Absence or narrowing of first part of small bowel | Not recorded |
| Intestinal malrotation | Not recorded |
| Jejunal atresia | Not recorded |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Accessory spleen | Rarely (1–4%) |
| Retinal vascular tortuosity | Not recorded |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Bilateral renal hypoplasia | Not recorded |
| Hydronephrosis | Not recorded |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Preaxial polydactyly | Rarely (1–4%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Low-set ears | Not recorded |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Muscle tissue disease | 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 CENPF and how often each is seen. Find out more at hpo.jax.org.
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