Trait
Crumpled ear
Distortion of the course of the normal folds of the ear and the appearance of supernumerary crura and folds.
Summary
- Body system
- Abnormality of the ear
Reference genomeGRCh38hg38
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Get my Genome Test6 genes linked to Crumpled ear
Changes in these genes cause rare conditions in which Crumpled ear 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 |
|---|---|---|
| UBAP2Lubiquitin associated protein 2 like | Always | In 1 condition |
| FBN2fibrillin 2 | Very often (80–99%) | In 2 conditions |
| LONP1lon peptidase 1, mitochondrial | Very often (80–99%) | In 2 conditions |
| FBN1fibrillin 1 | Often (30–79%) | In 1 condition |
| TWIST1twist family bHLH transcription factor 1 | Often (30–79%) | In 1 condition |
| MESDmesoderm development LRP chaperone | 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.
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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