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Trait

Short nasal bridge

Decreased superior-inferior length of the nasal bridge, which is the saddle-shaped area that includes the nasal root and the lateral aspects of the nose.

HPO HP:0003194

Summary

Also called
Decreased length of bridge of nose, Decreased length of nasal bridge, Short bridge of nose
Body system
Abnormality of head or neck

12 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.

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6 genes linked to Short nasal bridge

Changes in these genes cause rare conditions in which Short nasal bridge 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.

GeneHow often it is seenConditions
POMGNT1protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)AlwaysIn 1 condition
FGFR3fibroblast growth factor receptor 3Often (30–79%)In 1 condition
WDR26WD repeat domain 26Often (30–79%)In 1 condition
NR2F1nuclear receptor subfamily 2 group F member 1Sometimes (5–29%)In 1 condition
TRPV6transient receptor potential cation channel subfamily V member 6Sometimes (5–29%)In 1 condition
NOTCH3notch receptor 3Not recordedIn 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

Abnormality of the bridge of the nose

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 2026.10.19-9814e911.

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