OMOP Concept 37469530
Solitary congenital hypertrophy of retinal pigment epithelium
StandardConditionSNOMED1142277007Disorder
Maps from
1
Descendants
0
Valid from
1 Mar 2025
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Solitary congenital hypertrophy of retinal pigment epithelium via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| HPO | HP_0011528 | Solitary congenital hypertrophy of retinal pigment epithelium | Non-standard |
Synonyms
Alternative names recorded for Solitary congenital hypertrophy of retinal pigment epithelium across source vocabularies.
- hipertrofia congénita solitaria de epitelio pigmentario de retina
- hipertrofia congénita solitaria de epitelio pigmentario de retina (trastorno)
- hipertrofia congénita solitaria de epitelio pigmentario retiniano
- Solitary CHRPE (congenital hypertrophy of retinal pigment epithelium)
- Solitary congenital hypertrophy of retinal pigment epithelium (disorder)
- Unifocal CHRPE (congenital hypertrophy of retinal pigment epithelium)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(29)Roll up to these when you need a wider cohort.
- 1Congenital hypertrophy of retinal pigment epithelium
- 2Congenital anomaly of retina
- 2Retinal pigment epithelial hypertrophy
- 3Congenital anomaly of posterior segment of eye
- 3Retinal disorder
- 3Retinal pigment epithelial abnormality
- 4Anomaly of eye
- 4Congenital anomaly of eye
- 4Disorder of posterior segment of eye
- 4Disorder of vitreous body and/or retina
- 4Retina finding
- 5Congenital anomaly of head
- 5Congenital anomaly of visual system
- 5Disorder of eye
- 5Globe finding
- 6Congenital malformation
- 6Disorder of eye region
- 6Disorder of head
- 6Disorder of sensory organ
- 6Eye / vision finding
- 6Finding of head region
- 6Visual system disorder
- 7Clinical finding
- 7Congenital disease
- 7Developmental disorder
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