Trait
Midnasal stenosis
Abnormal narrowing (stenosis) of the midnasal cavity, i.e., of the middle nasal meatus, which in neonates can cause respiratory distress.
Summary
- Also called
- Midnasal atresia or stenosis
- Body system
- Abnormality of head or neck
Read the genes linked to Midnasal stenosis, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test16 genes linked to Midnasal stenosis
Changes in these genes cause rare conditions in which Midnasal stenosis 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 |
|---|---|---|
| CDONcell adhesion associated, oncogene regulated | Very often (80–99%) | In 1 condition |
| CRIPTOcripto, EGF-CFC family member | Very often (80–99%) | In 1 condition |
| DISP1dispatched RND transporter family member 1 | Very often (80–99%) | In 1 condition |
| DLL1delta like canonical Notch ligand 1 | Very often (80–99%) | In 1 condition |
| FGF8fibroblast growth factor 8 | Very often (80–99%) | In 1 condition |
| FGFR1fibroblast growth factor receptor 1 | Very often (80–99%) | In 1 condition |
| FOXH1forkhead box H1 | Very often (80–99%) | In 1 condition |
| GAS1growth arrest specific 1 | Very often (80–99%) | In 1 condition |
| GLI2GLI family zinc finger 2 | Very often (80–99%) | In 1 condition |
| NODALnodal growth differentiation factor | Very often (80–99%) | In 1 condition |
| PTCH1patched 1 | Very often (80–99%) | In 1 condition |
| SHHsonic hedgehog signaling molecule | Very often (80–99%) | In 2 conditions |
| SIX3SIX homeobox 3 | Very often (80–99%) | In 1 condition |
| SUFUSUFU negative regulator of hedgehog signaling | Very often (80–99%) | In 1 condition |
| TGIF1TGFB induced factor homeobox 1 | Very often (80–99%) | In 1 condition |
| ZIC2Zic family zinc finger 2 | Very often (80–99%) | 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.
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks