Trait
Vascular skin abnormality
Summary
- Also called
- Skin vascular malformation
Reference genomeGRCh38hg38
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Get my Genome Test10 genes linked to Vascular skin abnormality
Changes in these genes cause rare conditions in which Vascular skin abnormality 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 |
|---|---|---|
| ADA2adenosine deaminase 2 | Very often (80–99%) | In 1 condition |
| AKT1AKT serine/threonine kinase 1 | Very often (80–99%) | In 1 condition |
| NEU1neuraminidase 1 | Very often (80–99%) | In 1 condition |
| FUCA1alpha-L-fucosidase 1 | Often (30–79%) | In 1 condition |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Often (30–79%) | In 2 conditions |
| AGAaspartylglucosaminidase | Sometimes (5–29%) | In 1 condition |
| CCM2CCM2 scaffold protein | Sometimes (5–29%) | In 1 condition |
| KRIT1KRIT1 ankyrin repeat containing | Sometimes (5–29%) | In 1 condition |
| ODC1ornithine decarboxylase 1 | Sometimes (5–29%) | In 1 condition |
| PDCD10programmed cell death 10 | Sometimes (5–29%) | 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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