Trait
Oral white patch
Clinical name: Oral leukoplakia
A thickened white patch on the oral mucosa that cannot be rubbed off.
Summary
- Also called
- leukokeratosis, Oral idiopathic keratosis, Oral idiopathic leukoplakia, Oral idiopathic white patch, Oral leucoplakia, Oral leukokeratosis, Oral leukoplasia, Oral white plaque
- Body system
- Abnormality of head or neck
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Get my Genome Test27 genes linked to Oral white patch
Changes in these genes cause rare conditions in which Oral white patch 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 |
|---|---|---|
| DKC1dyskerin pseudouridine synthase 1 | Always | In 3 conditions |
| KRT16keratin 16 | Always | In 2 conditions |
| KRT4keratin 4 | Always | In 1 condition |
| KRT6Akeratin 6A | Always | In 3 conditions |
| TINF2TERF1 interacting nuclear factor 2 | Always | In 6 conditions |
| WRAP53WD repeat containing antisense to TP53 | Always | In 2 conditions |
| ACDACD shelterin complex subunit and telomerase recruitment factor | Very often (80–99%) | In 3 conditions |
| CTC1CST telomere replication complex component 1 | Very often (80–99%) | In 2 conditions |
| NHP2NHP2 ribonucleoprotein | Very often (80–99%) | In 2 conditions |
| NOP10NOP10 ribonucleoprotein | Very often (80–99%) | In 1 condition |
| NPM1nucleophosmin 1 | Very often (80–99%) | In 1 condition |
| PARNpoly(A)-specific ribonuclease | Very often (80–99%) | In 3 conditions |
| RTEL1regulator of telomere elongation helicase 1 | Very often (80–99%) | In 2 conditions |
| TERCtelomerase RNA component | Very often (80–99%) | In 3 conditions |
| TERTtelomerase reverse transcriptase | Very often (80–99%) | In 4 conditions |
| TYMSthymidylate synthetase | Very often (80–99%) | In 2 conditions |
| USB1U6 snRNA biogenesis phosphodiesterase 1 | Very often (80–99%) | In 1 condition |
| CASTcalpastatin | Often (30–79%) | In 1 condition |
| DCLRE1BDNA cross-link repair 1B | Often (30–79%) | In 1 condition |
| FERMT1FERM domain containing kindlin 1 | Often (30–79%) | In 1 condition |
| KRT17keratin 17 | Often (30–79%) | In 1 condition |
| KRT6Bkeratin 6B | Often (30–79%) | In 1 condition |
| MEFVMEFV innate immunity regulator, pyrin | Often (30–79%) | In 1 condition |
| KRT6Ckeratin 6C | Sometimes (5–29%) | In 1 condition |
| RPA1replication protein A1 | Sometimes (5–29%) | In 1 condition |
| GJB2gap junction protein beta 2 | Not recorded | In 1 condition |
| RHBDF2rhomboid 5 homolog 2 | 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.
Broader traits
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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