Trait
Difficulty opening the eyelids
Clinical name: Eyelid apraxia
Summary
Reference genomeGRCh38hg38
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Get my Genome Test5 genes linked to Difficulty opening the eyelids
Changes in these genes cause rare conditions in which Difficulty opening the eyelids 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 |
|---|---|---|
| PLA2G6phospholipase A2 group VI | Often (30–79%) | In 2 conditions |
| SYNJ1synaptojanin 1 | Often (30–79%) | In 1 condition |
| ATP13A2ATPase cation transporting 13A2 | Sometimes (5–29%) | In 1 condition |
| MAPTmicrotubule associated protein tau | Not recorded | In 1 condition |
| PANK2pantothenate kinase 2 | 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.
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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