OMOP Concept 37397260
Autosomal dominant optic atrophy classic form
StandardConditionSNOMED717336005Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Autosomal dominant optic atrophy classic form via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | D029241 | Optic Atrophy, Autosomal Dominant | Non-standard |
Synonyms
Alternative names recorded for Autosomal dominant optic atrophy classic form across source vocabularies.
- atrofia óptica autosómica dominante, forma clásica
- atrofia óptica autosómica dominante, forma clásica (trastorno)
- atrofia óptica autosómica dominante tipo Kjer
- Autosomal dominant optic atrophy classic form (disorder)
- Autosomal dominant optic atrophy Kjer type
- Kjer optic atrophy
- Optic atrophy type 1
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.
- 1Dominant hereditary optic atrophy
- 2Autosomal dominant hereditary disorder
- 2Hereditary optic atrophy
- 3Autosomal hereditary disorder
- 3Hereditary degenerative disease of central nervous system
- 3Inherited optic neuropathy
- 3Primary optic atrophy
- 4Degenerative disease of the central nervous system
- 4Disorder of optic nerve
- 4Hereditary disease
- 4Hereditary disorder of nervous system
- 4Hereditary disorder of the visual system
- 4Optic atrophy
- 5Cranial nerve disorder
- 5Degenerative disorder
- 5Disorder of nervous system
- 5Disorder of the central nervous system
- 5Disorder of visual pathways
- 5Genetic disease
- 5Hereditary disorder by system
- 5Visual system disorder
- 6Central nervous system finding
- 6Disease
- 6Disorder of body system
- 6Disorder of head
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