Trait

Abnormal chorioretinal morphology

An abnormality of the choroid and retina.

Also called: Chorioretinal abnormality
Body system: Abnormality of the eye

This page as data

Add .json to the page's address, or ask for application/json, to read it as JSON.

library(jsonlite)

url <- "https://dantelabs.com/traits/abnormal-chorioretinal-morphology.json"
page <- fromJSON(url)
page$trait$name

Open the JSON

Read the genes linked to Abnormal chorioretinal morphology, and the rest of your genome, with one test.

From $449Free shipping · Results in 6–8 weeks

Get my Genome Test

34 genes linked to Abnormal chorioretinal morphology

Changes in these genes cause rare conditions in which Abnormal chorioretinal 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
HLA-Amajor histocompatibility complex, class I, A	Very often (80–99%)	In 1 condition
NDPnorrin cystine knot growth factor NDP	Very often (80–99%)	In 1 condition
POU3F4POU class 3 homeobox 4	Very often (80–99%)	In 1 condition
B9D1B9 domain containing 1	Often (30–79%)	In 1 condition
B9D2B9 domain containing 2	Often (30–79%)	In 1 condition
CC2D2Acoiled-coil and C2 domain containing 2A	Often (30–79%)	In 1 condition
CEP290centrosomal protein 290	Often (30–79%)	In 1 condition
CSPP1centrosome and spindle pole associated protein 1	Often (30–79%)	In 1 condition
MKS1MKS transition zone complex subunit 1	Often (30–79%)	In 1 condition
PEX1peroxisomal biogenesis factor 1	Often (30–79%)	In 1 condition
PEX10peroxisomal biogenesis factor 10	Often (30–79%)	In 1 condition
PEX11Bperoxisomal biogenesis factor 11 beta	Often (30–79%)	In 1 condition
PEX12peroxisomal biogenesis factor 12	Often (30–79%)	In 1 condition
PEX13peroxisomal biogenesis factor 13	Often (30–79%)	In 1 condition
PEX14peroxisomal biogenesis factor 14	Often (30–79%)	In 1 condition
PEX16peroxisomal biogenesis factor 16	Often (30–79%)	In 1 condition
PEX19peroxisomal biogenesis factor 19	Often (30–79%)	In 1 condition
PEX2peroxisomal biogenesis factor 2	Often (30–79%)	In 1 condition
PEX26peroxisomal biogenesis factor 26	Often (30–79%)	In 1 condition
PEX3peroxisomal biogenesis factor 3	Often (30–79%)	In 1 condition
PEX5peroxisomal biogenesis factor 5	Often (30–79%)	In 1 condition
PEX6peroxisomal biogenesis factor 6	Often (30–79%)	In 1 condition
RPGRIP1RPGR interacting protein 1	Often (30–79%)	In 1 condition
RPGRIP1LRPGRIP1 like	Often (30–79%)	In 1 condition
TCTN1tectonic family member 1	Often (30–79%)	In 1 condition
TCTN2tectonic family member 2	Often (30–79%)	In 1 condition
TCTN3tectonic family member 3	Often (30–79%)	In 1 condition
TMEM107transmembrane protein 107	Often (30–79%)	In 1 condition
TMEM216transmembrane protein 216	Often (30–79%)	In 1 condition
TMEM231transmembrane protein 231	Often (30–79%)	In 1 condition
TMEM237transmembrane protein 237	Often (30–79%)	In 1 condition
TMEM67transmembrane protein 67	Often (30–79%)	In 1 condition
TXNDC15thioredoxin domain containing 15	Often (30–79%)	In 1 condition
HADHAhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	Sometimes (5–29%)	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

Abnormal choroid morphology Retina issue

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.