Trait
Impacted tooth
A tooth that has not erupted because of local impediments (overcrowding or fibrous gum overgrowth).
Summary
- Also called
- Buried tooth, Retained tooth
- Body system
- Abnormality of head or neck
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/impacted-tooth.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Impacted tooth, and the rest of your genome, with one test.
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Get my Genome Test10 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- X-linked Autoinflammatory DiseaseReads 1 of these genesIKBKGAbout this report →
- LipodystrophyReads 2 of these genesLMNAZMPSTE24About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Amelogenesis ImperfectaReads 1 of these genesFAM20AAbout this report →
Show 6 more reports
- Ectodermal DysplasiasReads 1 of these genesIKBKGAbout this report →
- VitreoretinopathyReads 1 of these genesIKBKGAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
- Other Inborn Errors of ImmunityReads 1 of these genesIKBKGAbout this report →
Read the genes linked to Impacted tooth, and the rest of your genome, with one test.
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Get my Genome Test5 genes linked to Impacted tooth
Changes in these genes cause rare conditions in which Impacted tooth 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 |
|---|---|---|
| CDH11cadherin 11 | Often (30–79%) | In 1 condition |
| FAM20AFAM20A golgi associated secretory pathway pseudokinase | Often (30–79%) | In 1 condition |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Sometimes (5–29%) | In 1 condition |
| LMNAlamin A/C | Sometimes (5–29%) | In 1 condition |
| ZMPSTE24zinc metallopeptidase STE24 | 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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