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Traits
Traits linked to MAG
myelin associated glycoprotein
The Human Phenotype Ontology links 34 traits to MAG, 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 |
|---|---|
| Abnormal pyramidal sign | Always |
| Babinski sign | Always |
| Global developmental delay | Always |
| Impaired distal vibration sensation | Always |
| Increased reflexes | Always |
| Lack of coordination of movement | Always |
| Impaired vibratory sensation | Very often (80–99%) |
| Intellectual disability | Very often (80–99%) |
| Decreased reflex response | Often (30–79%) |
| Loss of ability to walk | Often (30–79%) |
| Titubation | Sometimes (5–29%) |
| Ventriculomegaly | Sometimes (5–29%) |
| Cognitive impairment | Not recorded |
| Corpus callosum atrophy | Not recorded |
| Degeneration of cerebellum | Not recorded |
| Peripheral neuropathy | Not recorded |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Distal lower limb amyotrophy | Always |
| Involuntary muscle stiffness, contraction, or spasm | Always |
| Low muscle tone | Always |
| Low muscle tone, in neonatal onset | Always |
| Spastic dysarthria | Always |
| Spastic paraparesis | Always |
| Spastic walk | Always |
| Spastic paraplegia | Very often (80–99%) |
| Generalized decreased muscle tone | Often (30–79%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Astigmatism | Always |
| Decreased clarity of vision | Always |
| Farsightedness | Always |
| Involuntary, rapid, rhythmic eye movements | Always |
| Glaucoma | Often (30–79%) |
| Temporal optic disc pallor | Often (30–79%) |
| Optic atrophy | Not recorded |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Areflexia of lower limbs | Not recorded |
| Hyporeflexia of lower limbs | 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 MAG and how often each is seen. Find out more at hpo.jax.org.
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