OMOP Concept 4339016
X-linked retinitis pigmentosa
StandardConditionSNOMED232054005Disorder
Maps from
1
Descendants
3
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to X-linked retinitis pigmentosa via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 232054005 | X-linked retinitis pigmentosa | Non-standard |
Synonyms
Alternative names recorded for X-linked retinitis pigmentosa across source vocabularies.
- retinitis pigmentaria ligada al cromosoma X
- retinitis pigmentaria ligada al cromosoma X (trastorno)
- X-linked retinitis pigmentosa (disorder)
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.
- 1Retinitis pigmentosa
- 1X-linked hereditary disease
- 2Hereditary retinal dystrophy
- 2Sex-linked hereditary disorder
- 3Hereditary disease
- 3Hereditary disorder of the visual system
- 3Retinal dystrophy
- 4Degeneration of retina
- 4Genetic disease
- 4Hereditary disorder by system
- 4Visual system disorder
- 5Degenerative disorder of eye
- 5Disease
- 5Disorder of body system
- 5Eye / vision finding
- 5Retinal disorder
- 6Anomaly of eye
- 6Clinical finding
- 6Degenerative disorder
- 6Disorder of vitreous body and/or retina
- 6Retina finding
- 7Disorder of eye
- 7Disorder of posterior segment of eye
- 7Globe finding
- 8Disorder of eye region
Narrower concepts
(3)Included automatically when you query with descendants.
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