Trait
Metamorphopsia
A visual anomaly in which images appear distorted. A grid of straight lines appears wavy and parts of the grid may appear blank.
Summary
- Body system
- Abnormality of the eye
Reference genomeGRCh38hg38
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Get my Genome Test43 genes linked to Metamorphopsia
Changes in these genes cause rare conditions in which Metamorphopsia 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 |
|---|---|---|
| CRXcone-rod homeobox | Always | In 2 conditions |
| PRPH2peripherin 2 | Always | In 3 conditions |
| BEST1bestrophin 1 | Very often (80–99%) | In 1 condition |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Often (30–79%) | In 1 condition |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Often (30–79%) | In 1 condition |
| CFHcomplement factor H | Often (30–79%) | In 1 condition |
| CFIcomplement factor I | Often (30–79%) | In 1 condition |
| EFEMP1EGF-like fibulin extracellular matrix protein 1 | Often (30–79%) | In 1 condition |
| PRRT2proline rich transmembrane protein 2 | Often (30–79%) | In 1 condition |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Often (30–79%) | In 1 condition |
| ABCA4ATP binding cassette subfamily A member 4 | Sometimes (5–29%) | In 1 condition |
| ABCC6ATP binding cassette subfamily C member 6 | Sometimes (5–29%) | In 1 condition |
| ADAM9ADAM metallopeptidase domain 9 | Sometimes (5–29%) | In 1 condition |
| AIPL1AIP like 1 HSP90 co-chaperone | Sometimes (5–29%) | In 1 condition |
| ATF6activating transcription factor 6 | Sometimes (5–29%) | In 1 condition |
| CACNA1Fcalcium voltage-gated channel subunit alpha1 F | Sometimes (5–29%) | In 1 condition |
| CACNA2D4calcium voltage-gated channel auxiliary subunit alpha2delta 4 | Sometimes (5–29%) | In 1 condition |
| CDHR1cadherin related family member 1 | Sometimes (5–29%) | In 1 condition |
| CFAP410cilia and flagella associated protein 410 | Sometimes (5–29%) | In 1 condition |
| CFAP418cilia and flagella associated protein 418 | Sometimes (5–29%) | In 1 condition |
| CNGA3cyclic nucleotide gated channel subunit alpha 3 | Sometimes (5–29%) | In 1 condition |
| DRAM2DNA damage regulated autophagy modulator 2 | Sometimes (5–29%) | In 1 condition |
| ENPP1ectonucleotide pyrophosphatase/phosphodiesterase 1 | Sometimes (5–29%) | In 1 condition |
| FSD1Lfibronectin type III and SPRY domain containing 1 like | Sometimes (5–29%) | In 1 condition |
| GUCA1Aguanylate cyclase activator 1A | Sometimes (5–29%) | In 1 condition |
| GUCY2Dguanylate cyclase 2D, retinal | Sometimes (5–29%) | In 1 condition |
| MFSD8major facilitator superfamily domain containing 8 | Sometimes (5–29%) | In 1 condition |
| NMNAT1nicotinamide nucleotide adenylyltransferase 1 | Sometimes (5–29%) | In 1 condition |
| OPN1LWopsin 1, long wave sensitive | Sometimes (5–29%) | In 1 condition |
| OPN1MWopsin 1, medium wave sensitive | Sometimes (5–29%) | In 1 condition |
| PITPNM3PITPNM family member 3 | Sometimes (5–29%) | In 1 condition |
| POC1BPOC1 centriolar protein B | Sometimes (5–29%) | In 1 condition |
| PROM1prominin 1 | Sometimes (5–29%) | In 1 condition |
| RAB28RAB28, member RAS oncogene family | Sometimes (5–29%) | In 1 condition |
| RAX2retina and anterior neural fold homeobox 2 | Sometimes (5–29%) | In 1 condition |
| RIMS1regulating synaptic membrane exocytosis 1 | Sometimes (5–29%) | In 1 condition |
| RPGRretinitis pigmentosa GTPase regulator | Sometimes (5–29%) | In 1 condition |
| RPGRIP1RPGR interacting protein 1 | Sometimes (5–29%) | In 1 condition |
| SEMA4Asemaphorin 4A | Sometimes (5–29%) | In 1 condition |
| TLCD3BTLC domain containing 3B | Sometimes (5–29%) | In 1 condition |
Show 3 more genes
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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