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Traits
Traits linked to CEP104
centrosomal protein 104
The Human Phenotype Ontology links 47 traits to CEP104, 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 |
|---|---|
| Global developmental delay | Always |
| Head tremor | Always |
| Intellectual disability | Always |
| Molar tooth sign on MRI | Always |
| Unsteady walk | Always |
| Ataxia | Very often (80–99%) |
| Cerebellar vermis hypoplasia | Very often (80–99%) |
| Abnormal gait | Often (30–79%) |
| Abnormality of neuronal migration | Sometimes (5–29%) |
| Aplasia/Hypoplasia of the corpus callosum | Sometimes (5–29%) |
| Epilepsy | Sometimes (5–29%) |
| More grooves in brain | Sometimes (5–29%) |
| Self-biting | Sometimes (5–29%) |
| Too much cerebrospinal fluid in the brain | Sometimes (5–29%) |
| Tremor | Sometimes (5–29%) |
| Small cerebellum | Not recorded |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Decreased width of the skull | Often (30–79%) |
| Long face | Often (30–79%) |
| Cleft of the mouth | Sometimes (5–29%) |
| Encephalocele | Sometimes (5–29%) |
| Highly arched eyebrow | Sometimes (5–29%) |
| Nasal tip, upturned | Sometimes (5–29%) |
| Prominent nasal bridge | Sometimes (5–29%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Involuntary, rapid, rhythmic eye movements | Always |
| Oculomotor apraxia | Always |
| Abnormal electroretinogram | Often (30–79%) |
| Cat eye | Sometimes (5–29%) |
| Cross-eyed | Sometimes (5–29%) |
| Drooping upper eyelid | Sometimes (5–29%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Low muscle tone | Very often (80–99%) |
| Generalized decreased muscle tone | Often (30–79%) |
| Abnormal vertebral body morphology | Sometimes (5–29%) |
| Double-Jointed | Sometimes (5–29%) |
| Scoliosis | Sometimes (5–29%) |
Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Abnormal pattern of respiration | Very often (80–99%) |
| Apnea | Very often (80–99%) |
| Episodic tachypnea | Very often (80–99%) |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Duplication of bones of the toes | Sometimes (5–29%) |
| Extra finger | Sometimes (5–29%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Abnormal cardiovascular system morphology | Sometimes (5–29%) |
| All organs on wrong side of body | Sometimes (5–29%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Feeding difficulties in infancy | Often (30–79%) |
| Enlarged colon lacking nerve cells | Sometimes (5–29%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Low-set ears | Sometimes (5–29%) |
Abnormality of the endocrine system
| Trait | How often it is seen |
|---|---|
| Abnormality of the hypothalamus-pituitary axis | Sometimes (5–29%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Poor wound healing | Sometimes (5–29%) |
Abnormality of the voice
| Trait | How often it is seen |
|---|---|
| Nasal speech | Always |
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 CEP104 and how often each is seen. Find out more at hpo.jax.org.
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