Congenital anomalies of posterior segment of eye
753.2
Congenital Anomalies
Both
752-754.99
ICD mappings
| ICD code | Type | Description | Phenome |
|---|---|---|---|
| Q14 | ICD10CM | Congenital malformations of posterior segment of eye | MGI |
| Q14.0 | ICD10CM | Congenital malformation of vitreous humor | MGI |
| Q14.1 | ICD10CM | Congenital malformation of retina | MGI |
| Q14.2 | ICD10CM | Congenital malformation of optic disc | MGI |
| Q14.3 | ICD10CM | Congenital malformation of choroid | MGI |
| Q14.8 | ICD10CM | Other congenital malformations of posterior segment of eye | MGI |
| Q14.9 | ICD10CM | Congenital malformation of posterior segment of eye, unspecified | MGI |
| 743.51 | ICD9CM | Vitreous anomalies | MGI |
| 743.52 | ICD9CM | Fundus coloboma | MGI |
| 743.53 | ICD9CM | Chorioretinal degeneration, congenital | MGI |
| 743.54 | ICD9CM | Congenital folds and cysts of posterior segment | MGI |
| 743.55 | ICD9CM | Congenital macular changes | MGI |
| 743.56 | ICD9CM | Other retinal changes, congenital | MGI |
| 743.57 | ICD9CM | Specified congenital anomalies of optic disc | MGI |
| 743.58 | ICD9CM | Vascular anomalies | MGI |
| 743.59 | ICD9CM | Other congenital anomalies of posterior segment | MGI |
| Q14.0 | ICD10 | Q14.0 Congenital malformation of vitreous humour | UKB |
| Q14.1 | ICD10 | Q14.1 Congenital malformation of retina | UKB |
| Q14.8 | ICD10 | Q14.8 Other congenital malformations of posterior segment of eye | UKB |
| Q14.9 | ICD10 | Q14.9 Congenital malformation of posterior segment of eye, unspecified | UKB |
| 743.5 | ICD9 | 7435 Congenital anomalies of posterior segment | UKB |
| 743.51 | ICD9 | 74351 Specified anomalies of retina | UKB |
| 743.52 | ICD9 | 74352 Specified anomalies of optic disc | UKB |
| 743.53 | ICD9 | 74353 Specified anomalies of choroid | UKB |
| 743.59 | ICD9 | 74359 Congenital anomalies of posterior segment (other and unspecified) | UKB |
This page is mainly a phenotype dictionary entry. When you are trying to find candidate PRS models, go to the Scores table, search by trait or exposure name, and then use the score-detail and PheWAS pages for model-specific follow-up.