Trait
Thick nail
Clinical name: Onychogryphosis
Onychogryphosis is a disorder of nail plate growth that is clinically characterized by an opaque, yellow-brown thickening of the nail plate with associated gross hyperkeratosis, elongation, and increased curvature.
Summary
- Also called
- Thickened nails, Dystrophic thickened nails, Onychogryposis
- Body system
- Abnormality of the integument
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/onychogryphosis.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Thick nail, and the rest of your genome, with one test.
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Get my Genome Test19 genes linked to Thick nail
Changes in these genes cause rare conditions in which Thick nail 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 |
|---|---|---|
| ADAM17ADAM metallopeptidase domain 17 | Always | In 2 conditions |
| ITGB4integrin subunit beta 4 | Always | In 1 condition |
| LMNAlamin A/C | Always | In 1 condition |
| COL7A1collagen type VII alpha 1 chain | Very often (80–99%) | In 1 condition |
| CTSCcathepsin C | Often (30–79%) | In 2 conditions |
| HPGD15-hydroxyprostaglandin dehydrogenase | Often (30–79%) | In 1 condition |
| KRT83keratin 83 | Often (30–79%) | In 1 condition |
| WDR19WD repeat domain 19 | Often (30–79%) | In 1 condition |
| FZD6frizzled class receptor 6 | Sometimes (5–29%) | In 1 condition |
| GJB2gap junction protein beta 2 | Sometimes (5–29%) | In 1 condition |
| GJB6gap junction protein beta 6 | Sometimes (5–29%) | In 1 condition |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Sometimes (5–29%) | In 2 conditions |
| KRT14keratin 14 | Sometimes (5–29%) | In 1 condition |
| KRT5keratin 5 | Sometimes (5–29%) | In 2 conditions |
| LORICRINloricrin cornified envelope precursor protein | Sometimes (5–29%) | In 1 condition |
| KRT16keratin 16 | Not recorded | In 1 condition |
| KRT6Akeratin 6A | Not recorded | In 1 condition |
| TP63tumor protein p63 | Not recorded | In 1 condition |
| ZSWIM6zinc finger SWIM-type containing 6 | 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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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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