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Traits
Traits linked to MOG
myelin oligodendrocyte glycoprotein
The Human Phenotype Ontology links 32 traits to MOG, 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 |
|---|---|
| Cataplexy | Always |
| Excessive daytime sleepiness | Always |
| Difficulty sleeping | Very often (80–99%) |
| Hallucinations | Very often (80–99%) |
| Transient global amnesia | Very often (80–99%) |
| Abnormal rapid eye movement sleep | Often (30–79%) |
| Anxiety | Often (30–79%) |
| Attention deficit | Often (30–79%) |
| Hypnagogic hallucination | Often (30–79%) |
| Hypnopompic hallucination | Often (30–79%) |
| NREM parasomnia | Often (30–79%) |
| Obstructive sleep apnea | Often (30–79%) |
| Sleep paralysis | Often (30–79%) |
| Willis-Ekbom disease | Often (30–79%) |
| Depression | Sometimes (5–29%) |
| Migraine | Sometimes (5–29%) |
| Pauses in breathing while sleeping | Sometimes (5–29%) |
| Restlessness | Sometimes (5–29%) |
| Slurred speech | Sometimes (5–29%) |
| Psychosis | Rarely (1–4%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Female sexual dysfunction | Often (30–79%) |
| Male sexual dysfunction | Often (30–79%) |
| Nocturia | Often (30–79%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| High blood pressure | Often (30–79%) |
| Fainting spell | Sometimes (5–29%) |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Drooling | Often (30–79%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Constipation | Often (30–79%) |
Abnormality of the endocrine system
| Trait | How often it is seen |
|---|---|
| Early onset of puberty | Sometimes (5–29%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Abnormal pupillary function | Often (30–79%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Excessive sweating | Often (30–79%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Obesity | Very often (80–99%) |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Noninsulin-dependent diabetes | 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 MOG and how often each is seen. Find out more at hpo.jax.org.
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