Trait
Abnormal choroid morphology
Any structural abnormality of the choroid (the posterior part of the uvea, the middle tunic of the eye, consisting mainly of blood vessels).
Summary
- Also called
- Abnormality of the choroid
- Body system
- Abnormality of the eye
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Abnormal choroid morphology, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test22 genes linked to Abnormal choroid morphology
Changes in these genes cause rare conditions in which Abnormal choroid morphology 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 |
|---|---|---|
| ABCA4ATP binding cassette subfamily A member 4 | Very often (80–99%) | In 1 condition |
| ALDH1A3aldehyde dehydrogenase 1 family member A3 | Very often (80–99%) | In 1 condition |
| BEST1bestrophin 1 | Very often (80–99%) | In 1 condition |
| CNGB3cyclic nucleotide gated channel subunit beta 3 | Very often (80–99%) | In 1 condition |
| CRB1crumbs cell polarity complex component 1 | Very often (80–99%) | In 1 condition |
| ELOVL4ELOVL fatty acid elongase 4 | Very often (80–99%) | In 1 condition |
| HLA-Amajor histocompatibility complex, class I, A | Very often (80–99%) | In 1 condition |
| MFRPmembrane frizzled-related protein | Very often (80–99%) | In 1 condition |
| OTX2orthodenticle homeobox 2 | Very often (80–99%) | In 1 condition |
| PROM1prominin 1 | Very often (80–99%) | In 1 condition |
| PRPH2peripherin 2 | Very often (80–99%) | In 1 condition |
| PRSS56serine protease 56 | Very often (80–99%) | In 1 condition |
| RAXretina and anterior neural fold homeobox | Very often (80–99%) | In 1 condition |
| SIX6SIX homeobox 6 | Very often (80–99%) | In 1 condition |
| SOX2SRY-box transcription factor 2 | Very often (80–99%) | In 1 condition |
| TMEM98transmembrane protein 98 | Very often (80–99%) | In 1 condition |
| TIMP3TIMP metallopeptidase inhibitor 3 | Often (30–79%) | In 1 condition |
| GNAQG protein subunit alpha q | Sometimes (5–29%) | In 1 condition |
| NF1neurofibromin 1 | Sometimes (5–29%) | In 1 condition |
| NOD2nucleotide binding oligomerization domain containing 2 | Sometimes (5–29%) | In 1 condition |
| RLBP1retinaldehyde binding protein 1 | Sometimes (5–29%) | In 1 condition |
| CLCNKBchloride voltage-gated channel Kb | 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.
Narrower traits
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.
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks