Trait
Progressive drooping of upper eyelid
Clinical name: Progressive ptosis
A progressive form of ptosis.
Summary
- Body system
- Abnormality of the eye
Reference genomeGRCh38hg38
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Read the genes linked to Progressive drooping of upper eyelid, and the rest of your genome, with one test.
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Get my Genome Test7 genes linked to Progressive drooping of upper eyelid
Changes in these genes cause rare conditions in which Progressive drooping of upper eyelid 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 |
|---|---|---|
| PABPN1poly(A) binding protein nuclear 1 | Always | In 1 condition |
| ABCD3ATP binding cassette subfamily D member 3 | Very often (80–99%) | In 1 condition |
| GIPC1GIPC PDZ domain containing family member 1 | Very often (80–99%) | In 1 condition |
| LRP12LDL receptor related protein 12 | Very often (80–99%) | In 1 condition |
| NOTCH2NLCnotch 2 N-terminal like C | Very often (80–99%) | In 1 condition |
| NUTM2B-AS1NUTM2B antisense RNA 1 | Very often (80–99%) | In 1 condition |
| RILPL1Rab interacting lysosomal protein like 1 | 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.
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