Trait

Completely dislocated lens

Clinical name: Lens luxation

Complete dislocation of the lens of the eye.

HPO HP:0012019

Also called: Completely dislocated lenses
Body system: Abnormality of the eye

This page as data

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8 genes linked to Completely dislocated lens

Changes in these genes cause rare conditions in which Completely dislocated lens 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
FBN1fibrillin 1	Always	In 1 condition
GNAQG protein subunit alpha q	Often (30–79%)	In 1 condition
COL2A1collagen type II alpha 1 chain	Sometimes (5–29%)	In 1 condition
PAX2paired box 2	Sometimes (5–29%)	In 1 condition
C12orf57chromosome 12 open reading frame 57	Not recorded	In 1 condition
COL11A1collagen type XI alpha 1 chain	Not recorded	In 1 condition
MOCS1molybdenum cofactor synthesis 1	Not recorded	In 1 condition
MOCS2molybdenum cofactor synthesis 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

Ectopia lentis

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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