OMOP Concept 4048740
Dominant hereditary optic atrophy
StandardConditionSNOMED2065009Disorder
Maps from
1
Descendants
5
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Dominant hereditary optic atrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 141807 | Dominant hereditary optic atrophy | Non-standard |
Synonyms
Alternative names recorded for Dominant hereditary optic atrophy across source vocabularies.
- atrofia óptica hereditaria dominante
- atrofia óptica hereditaria dominante (trastorno)
- Autosomal dominant optic atrophy
- Dominant hereditary optic atrophy (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.
- 1Autosomal dominant hereditary disorder
- 1Hereditary optic atrophy
- 2Autosomal hereditary disorder
- 2Hereditary degenerative disease of central nervous system
- 2Inherited optic neuropathy
- 2Primary optic atrophy
- 3Degenerative disease of the central nervous system
- 3Disorder of optic nerve
- 3Hereditary disease
- 3Hereditary disorder of nervous system
- 3Hereditary disorder of the visual system
- 3Optic atrophy
- 4Cranial nerve disorder
- 4Degenerative disorder
- 4Disorder of nervous system
- 4Disorder of the central nervous system
- 4Disorder of visual pathways
- 4Genetic disease
- 4Hereditary disorder by system
- 4Visual system disorder
- 5Central nervous system finding
- 5Disease
- 5Disorder of body system
- 5Disorder of head
- 5Eye / vision finding
Showing 25 of 29. Retrieve the full set via the API.
Narrower concepts
(5)Included automatically when you query with descendants.
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