OMOP Concept 4180280
Congenital hypoplasia of fovea centralis
StandardConditionSNOMED429449002Disorder
Maps from
1
Descendants
2
Valid from
31 Jan 2008
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Congenital hypoplasia of fovea centralis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| HPO | HP_0007750 | Hypoplasia of the fovea | Non-standard |
Synonyms
Alternative names recorded for Congenital hypoplasia of fovea centralis across source vocabularies.
- Congenital hypoplasia of fovea
- Congenital hypoplasia of fovea centralis (disorder)
- hipoplasia congénita de mácula
- hipoplasia congénita de mácula (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(32)Roll up to these when you need a wider cohort.
- 1Congenital hypoplasia of macula lutea
- 1Structural abnormality of fovea centralis
- 2Anomaly of eye
- 2Congenital anomaly of macula
- 2Congenital hypoplasia of retina
- 2Disorder of macula of retina
- 3Congenital anomaly of retina
- 3Disorder of eye
- 3Macula finding
- 3Retinal disorder
- 4Congenital anomaly of posterior segment of eye
- 4Disorder of eye region
- 4Disorder of sensory organ
- 4Disorder of vitreous body and/or retina
- 4Globe finding
- 4Retina finding
- 5Congenital anomaly of eye
- 5Disease
- 5Disorder of head
- 5Disorder of posterior segment of eye
- 5Eye / vision finding
- 5Finding of head region
- 5Visual system disorder
- 6Clinical finding
- 6Congenital anomaly of head
Showing 25 of 32. Retrieve the full set via the API.
Narrower concepts
(2)Included automatically when you query with descendants.
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