AtlasTrait
Narrowing of windpipe
Clinical name: Tracheal stenosis
Summary
- Body system
- Abnormality of the respiratory system
AtlasThis 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/tracheal-stenosis.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Narrowing of windpipe, and the rest of your genome, with one test.
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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.
- Mowat-Wilson SyndromeReads 1 of these genesZEB2About this report →
- Mucopolysaccharidosis Type I (Hurler and Scheie Syndromes)Reads 1 of these genesIDUAAbout this report →
- Pendred SyndromeReads 1 of these genesSLC26A4About this report →
- Smith-Lemli-Opitz SyndromeReads 1 of these genesDHCR7About this report →
Show 13 more reports
- Immuno-Osseous DysplasiasReads 1 of these genesRMRPAbout this report →
- Renal Tubular AcidosisReads 1 of these genesFOXI1About this report →
- Marfan Like SyndromesReads 1 of these genesFBN1About this report →
- Familial HypomagnesemiaReads 1 of these genesKCNJ10About this report →
- Aortic AneurysmReads 1 of these genesFBN1About this report →
- Congenital HypothyroidismReads 1 of these genesSLC26A4About this report →
- Thyroid CancerReads 1 of these genesSLC26A4About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesKCNJ10About this report →
- Lysosomal Storage DiseaseReads 1 of these genesIDUAAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesSLC26A4About this report →
- Epilepsy (Full Panel)Reads 1 of these genesZEB2About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesRMRPAbout this report →
- Intellectual DisabilityReads 1 of these genesZEB2About this report →
Read the genes linked to Narrowing of windpipe, and the rest of your genome, with one test.
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Get my Genome Test26 genes linked to Narrowing of windpipe
Changes in these genes cause rare conditions in which Narrowing of windpipe 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 |
|---|---|---|
| BUB1BUB1 mitotic checkpoint serine/threonine kinase | Always | In 1 condition |
| HOXD13homeobox D13 | Very often (80–99%) | In 1 condition |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Very often (80–99%) | In 1 condition |
| DHCR77-dehydrocholesterol reductase | Often (30–79%) | In 1 condition |
| HYLS1HYLS1 centriolar and ciliogenesis associated | Often (30–79%) | In 1 condition |
| RSPO2R-spondin 2 | Often (30–79%) | In 1 condition |
| TBX4T-box transcription factor 4 | Often (30–79%) | In 1 condition |
| WNT3Wnt family member 3 | Often (30–79%) | In 1 condition |
| ADAMTSL2ADAMTS like 2 | Sometimes (5–29%) | In 2 conditions |
| ARSLarylsulfatase L | Sometimes (5–29%) | In 1 condition |
| DDRGK1DDRGK domain containing 1 | Sometimes (5–29%) | In 1 condition |
| FBN1fibrillin 1 | Sometimes (5–29%) | In 1 condition |
| FOXI1forkhead box I1 | Sometimes (5–29%) | In 1 condition |
| FRAS1Fraser extracellular matrix complex subunit 1 | Sometimes (5–29%) | In 1 condition |
| FREM2FRAS1 related extracellular matrix 2 | Sometimes (5–29%) | In 1 condition |
| GRIP1glutamate receptor interacting protein 1 | Sometimes (5–29%) | In 1 condition |
| KCNJ10potassium inwardly rectifying channel subfamily J member 10 | Sometimes (5–29%) | In 1 condition |
| LTBP3latent transforming growth factor beta binding protein 3 | Sometimes (5–29%) | In 2 conditions |
| PCNTpericentrin | Sometimes (5–29%) | In 1 condition |
| SLC26A4solute carrier family 26 member 4 | Sometimes (5–29%) | In 1 condition |
| SOX9SRY-box transcription factor 9 | Sometimes (5–29%) | In 1 condition |
| ZEB2zinc finger E-box binding homeobox 2 | Rarely (1–4%) | In 2 conditions |
| EBPEBP cholestenol delta-isomerase | Not recorded | In 1 condition |
| FLNBfilamin B | Not recorded | In 1 condition |
| IDUAalpha-L-iduronidase | Not recorded | In 1 condition |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | 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 2026.10.17-8666dff2.
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