OMOP Concept 378547
Congenital anomaly of retina
StandardConditionSNOMED49381001Disorder
Maps from
14
Descendants
101
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
14 source codes normalize to Congenital anomaly of retina via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 144194 | Congenital anomaly of retina | Non-standard |
| CIM10 | Q14.1 | Congenital malformation of retina | Non-standard |
| ICD10 | Q14.1 | Congenital malformation of retina | Non-standard |
| ICD10CM | Q14.1 | Congenital malformation of retina | Non-standard |
| ICD10CN | Q14.1 | Congenital malformation of retina | Non-standard |
| ICD10CN | Q14.100 | Congenital malformation of retina | Non-standard |
| ICD10CN | Q14.101 | Retinal dysplasia (machine translation) | Non-standard |
| ICD10CN | Q14.102 | Congenital retinal pigment abnormalities (machine translation) | Non-standard |
| ICD10CN | Q14.103 | Congenital retinal aneurysm (machine translation) | Non-standard |
| ICD10GM | Q14.1 | Congenital malformation of retina | Non-standard |
| ICD9CM | 743.56 | Other retinal changes, congenital | Non-standard |
| KCD7 | Q14.1 | Congenital malformation of retina | Non-standard |
| Read | P355.00 | Other congenital retinal changes | Non-standard |
| Read | P355z00 | Other congenital retinal changes NOS | Non-standard |
Synonyms
Alternative names recorded for Congenital anomaly of retina across source vocabularies.
- anomalía congénita de la retina
- anomalía congénita de la retina (trastorno)
- Congenital anomaly of retina (disorder)
- Congenital malformation of retina
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(25)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of posterior segment of eye
- 1Retinal disorder
- 2Congenital anomaly of eye
- 2Disorder of posterior segment of eye
- 2Disorder of vitreous body and/or retina
- 2Retina finding
- 3Anomaly of eye
- 3Congenital anomaly of head
- 3Congenital anomaly of visual system
- 3Disorder of eye
- 3Globe finding
- 4Congenital malformation
- 4Disorder of eye region
- 4Disorder of head
- 4Disorder of sensory organ
- 4Eye / vision finding
- 4Finding of head region
- 4Visual system disorder
- 5Clinical finding
- 5Congenital disease
- 5Developmental disorder
- 5Disease
- 5Disorder of body system
- 5Head finding
- 6Fetal and/or neonatal disorder
Narrower concepts
(101)Included automatically when you query with descendants.
- 1Achromatopsia
- 1Albinotic fundus
- 1Amaurosis hypertrichosis syndrome
- 1Atypical Norrie disease due to monosomy Xp11.3
- 1Blue cone monochromatism
- 1Cholestasis with pigmentary retinopathy and cleft palate syndrome
- 1Cleft lip retinopathy syndrome
- 1Coloboma of retina
- 1Congenital anomaly of left retina
- 1Congenital anomaly of macula
- 1Congenital anomaly of optic disc
- 1Congenital anomaly of right retina
- 1Congenital chorioretinal degeneration
- 1Congenital hypertrophy of retinal pigment epithelium
- 1Congenital hypoplasia of retina
- 1Congenital retinal aneurysm
- 1Congenital retinal fold
- 1Congenital retinoschisis
- 1Congenital stationary night blindness
- 1Congenital stricture of retinal artery
- 1Encephalopathy, intracerebral calcification, retinal degeneration syndrome
- 1Myelinated nerve fiber layer of retina
- 1Oculocutaneous albinism type 8
- 1Oculotrichodysplasia
- 1Oliver McFarlane syndrome
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