Trait
Abnormal corticospinal tract morphology
Abnormality of the corticospinal tract, which is the chief element of the pyramidal system (the principle motor tract) and is the only direct connection between the cerebrum and the spinal cord.
Summary
- Also called
- Morphological abnormality of the corticospinal tract
- Body system
- Abnormality of the nervous system
Reference genomeGRCh38hg38
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Get my Genome Test6 genes linked to Abnormal corticospinal tract morphology
Changes in these genes cause rare conditions in which Abnormal corticospinal tract morphology is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| DCCDCC netrin 1 receptor | Often (30–79%) | In 1 condition |
| DNAL4dynein axonemal light chain 4 | Often (30–79%) | In 1 condition |
| NTN1netrin 1 | Often (30–79%) | In 1 condition |
| RAD51RAD51 recombinase | Often (30–79%) | In 1 condition |
| GALCgalactosylceramidase | Rarely (1–4%) | In 1 condition |
| ALS2alsin Rho guanine nucleotide exchange factor ALS2 | Not recorded | In 1 condition |
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.
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Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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