OMOP Concept 44782850
Hereditary retinal dystrophy primarily involving retinal pigment epithelium
StandardConditionSNOMED698847000Disorder
Maps from
0
Descendants
6
Valid from
31 Jan 2014
Valid to
31 Dec 2099
OMOP concepts
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Synonyms
Alternative names recorded for Hereditary retinal dystrophy primarily involving retinal pigment epithelium across source vocabularies.
- distrofia hereditaria de la retina que afecta principalmente al epitelio pigmentario
- distrofia hereditaria de la retina que afecta principalmente al epitelio pigmentario (trastorno)
- Hereditary retinal dystrophy primarily involving retinal pigment epithelium (disorder)
- Inherited retinal dystrophy primarily involving retinal pigment epithelium
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(28)Roll up to these when you need a wider cohort.
- 1Hereditary retinal dystrophy
- 1Retinal pigment epithelial dystrophy
- 2Hereditary disorder of the visual system
- 2Retinal dystrophy
- 2Retinal pigment epithelial abnormality
- 3Anomaly of eye
- 3Degeneration of retina
- 3Hereditary disorder by system
- 3Retinal disorder
- 3Visual system disorder
- 4Degenerative disorder of eye
- 4Disorder of body system
- 4Disorder of eye
- 4Disorder of vitreous body and/or retina
- 4Eye / vision finding
- 4Hereditary disease
- 4Retina finding
- 5Clinical finding
- 5Degenerative disorder
- 5Disease
- 5Disorder of eye region
- 5Disorder of posterior segment of eye
- 5Disorder of sensory organ
- 5Genetic disease
- 5Globe finding
Showing 25 of 28. Retrieve the full set via the API.
Narrower concepts
(6)Included automatically when you query with descendants.
- 1Biallelic RPE65 mutation associated retinal dystrophy
- 1Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus
- 1Pattern dystrophy of macula
- 1Reticular dystrophy of retinal pigment epithelium
- 2Butterfly-shaped pigmentary macular dystrophy
- 2Martinique crinkled retinal pigment epitheliopathy
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