OMOP Concept 36716433
Ectopia lentis, chorioretinal dystrophy, myopia syndrome
StandardConditionSNOMED722437006Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Ectopia lentis, chorioretinal dystrophy, myopia syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536124 | Noble Bass Sherman syndrome | Non-standard |
| Nebraska Lexicon | 722437006 | Ectopia lentis, chorioretinal dystrophy, myopia syndrome | Non-standard |
Synonyms
Alternative names recorded for Ectopia lentis, chorioretinal dystrophy, myopia syndrome across source vocabularies.
- Ectopia lentis, chorioretinal dystrophy, myopia syndrome (disorder)
- síndrome de ectopia de cristalino, distrofia coriorretiniana y miopía
- síndrome de ectopia de cristalino, distrofia coriorretiniana y miopía (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(54)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital chorioretinal degeneration
- 1Congenital ectopic lens
- 1Developmental hereditary disorder
- 1Hereditary disorder of the visual system
- 1Retinal dystrophy
- 2Autosomal hereditary disorder
- 2Chorioretinal degeneration
- 2Congenital anomaly of choroid
- 2Congenital anomaly of lens
- 2Congenital anomaly of retina
- 2Degeneration of retina
- 2Developmental disorder
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Lesion of eye
- 2Visual system disorder
- 3Anomaly of eye
- 3Chorioretinal disorder
- 3Choroidal degeneration
- 3Congenital anomaly of anterior segment of eye
- 3Congenital anomaly of posterior segment of eye
- 3Degenerative disorder of eye
- 3Disease
- 3Disorder of body system
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