Trait
Exodeviation
A manifest or latent ocular deviation in which one or both eyes tends to deviate temporally.
Summary
- Also called
- Divergent strabismus
- Body system
- Abnormality of the eye
Reference genomeGRCh38hg38
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Get my Genome Test17 genes linked to Exodeviation
Changes in these genes cause rare conditions in which Exodeviation 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 |
|---|---|---|
| ALPK3alpha kinase 3 | Always | In 1 condition |
| DHRS3dehydrogenase/reductase 3 | Always | In 1 condition |
| FGFR2fibroblast growth factor receptor 2 | Always | In 1 condition |
| GMPPAGDP-mannose pyrophosphorylase A | Always | In 1 condition |
| GRIA1glutamate ionotropic receptor AMPA type subunit 1 | Always | In 1 condition |
| IFT27intraflagellar transport 27 | Always | In 1 condition |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Always | In 1 condition |
| ATP13A2ATPase cation transporting 13A2 | Often (30–79%) | In 1 condition |
| CDH11cadherin 11 | Often (30–79%) | In 1 condition |
| HMX1H6 family homeobox 1 | Often (30–79%) | In 1 condition |
| MRPS2mitochondrial ribosomal protein S2 | Often (30–79%) | In 1 condition |
| NRLneural retina leucine zipper | Often (30–79%) | In 1 condition |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Sometimes (5–29%) | In 1 condition |
| HPDL4-hydroxyphenylpyruvate dioxygenase like | Sometimes (5–29%) | In 1 condition |
| MTRFRmitochondrial translation release factor in rescue | Sometimes (5–29%) | In 1 condition |
| NEDD4LNEDD4 like E3 ubiquitin protein ligase | Sometimes (5–29%) | In 1 condition |
| AFG2AAAA ATPase AFG2A | Rarely (1–4%) | 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.
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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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