OMOP Concept 36715503
Early-onset X-linked optic atrophy
StandardConditionSNOMED721200000Disorder
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 Early-onset X-linked optic atrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537125 | Optic atrophy, X-linked | Non-standard |
| Nebraska Lexicon | 721200000 | Optic atrophy type 2 | Non-standard |
Synonyms
Alternative names recorded for Early-onset X-linked optic atrophy across source vocabularies.
- atrofia óptica de comienzo temprano ligada al cromosoma X
- atrofia óptica de comienzo temprano ligada al cromosoma X (trastorno)
- atrofia óptica tipo 2
- Early-onset X-linked optic atrophy (disorder)
- Non-Leber type optic atrophy with early-onset
- Optic atrophy type 2
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(30)Roll up to these when you need a wider cohort.
- 1Congenital atrophy of optic nerve
- 1X-linked optic atrophy
- 2Congenital disease
- 2Hereditary optic atrophy
- 2Optic atrophy
- 2X-linked hereditary disease
- 3Degenerative disease of the central nervous system
- 3Disorder of fetus and/or newborn
- 3Disorder of optic nerve
- 3Hereditary degenerative disease of central nervous system
- 3Inherited optic neuropathy
- 3Primary optic atrophy
- 3Sex-linked hereditary disorder
- 4Cranial nerve disorder
- 4Degenerative disorder
- 4Disease
- 4Disorder of the central nervous system
- 4Disorder of visual pathways
- 4Hereditary disease
- 4Hereditary disorder of nervous system
- 4Hereditary disorder of the visual system
- 5Central nervous system finding
- 5Clinical finding
- 5Disorder of nervous system
- 5Genetic disease
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