Trait
Abnormal epidermal morphology
An abnormality of the morphology of the epidermis.
Summary
- Also called
- Abnormality of epidermal morphology
- Body system
- Abnormality of the integument
Reference genomeGRCh38hg38
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Get my Genome Test4 genes linked to Abnormal epidermal morphology
Changes in these genes cause rare conditions in which Abnormal epidermal 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 |
|---|---|---|
| AAGABalpha and gamma adaptin binding protein | Very often (80–99%) | In 1 condition |
| COL14A1collagen type XIV alpha 1 chain | Very often (80–99%) | In 1 condition |
| LRP1LDL receptor related protein 1 | Very often (80–99%) | In 1 condition |
| CYP26C1cytochrome P450 family 26 subfamily C member 1 | Often (30–79%) | 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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