OMOP Concept 373206
Hereditary optic atrophy
StandardConditionSNOMED26360005Disorder
Maps from
6
Descendants
30
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
6 source codes normalize to Hereditary optic atrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138752 | Hereditary optic atrophy | Non-standard |
| ICD10CM | H47.22 | Hereditary optic atrophy | Non-standard |
| ICD9CM | 377.16 | Hereditary optic atrophy | Non-standard |
| MeSH | D015418 | Optic Atrophies, Hereditary | Non-standard |
| Read | F4H1700 | Hereditary optic atrophy NOS | Non-standard |
| Read | P2xz100 | Congenital optic atrophy | Non-standard |
Synonyms
Alternative names recorded for Hereditary optic atrophy across source vocabularies.
- atrofia óptica hereditaria
- atrofia óptica hereditaria (trastorno)
- Hereditary optic atrophy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(26)Roll up to these when you need a wider cohort.
- 1Hereditary degenerative disease of central nervous system
- 1Inherited optic neuropathy
- 1Primary optic atrophy
- 2Degenerative disease of the central nervous system
- 2Disorder of optic nerve
- 2Hereditary disorder of nervous system
- 2Hereditary disorder of the visual system
- 2Optic atrophy
- 3Cranial nerve disorder
- 3Degenerative disorder
- 3Disorder of nervous system
- 3Disorder of the central nervous system
- 3Disorder of visual pathways
- 3Hereditary disorder by system
- 3Visual system disorder
- 4Central nervous system finding
- 4Disease
- 4Disorder of body system
- 4Disorder of head
- 4Eye / vision finding
- 4Finding of head region
- 4Hereditary disease
- 4Neuropathy
- 5Clinical finding
- 5Genetic disease
Showing 25 of 26. Retrieve the full set via the API.
Narrower concepts
(30)Included automatically when you query with descendants.
- 1Arts syndrome
- 1Autosomal recessive optic atrophy type 6
- 1Autosomal recessive optic atrophy type 7
- 1Childhood-onset autosomal dominant optic atrophy
- 1Dominant hereditary optic atrophy
- 1Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome
- 1Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome
- 1Hereditary left optic atrophy
- 1Hereditary motor and sensory neuropathy with optic atrophy
- 1Hereditary right optic atrophy
- 1Infantile cerebellar and retinal degeneration
- 1Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome
- 1Leber's optic atrophy
- 1MEPAN syndrome
- 1SPOAN and SPOAN-related disorder
- 1Wolfram-like syndrome
- 1X-linked optic atrophy
- 2Autosomal dominant optic atrophy and cataract
- 2Autosomal dominant optic atrophy and peripheral neuropathy syndrome
- 2Autosomal dominant optic atrophy classic form
- 2Autosomal dominant optic atrophy plus syndrome
- 2Autosomal recessive spastic paraplegia type 55
- 2Autosomal recessive spastic paraplegia type 57
- 2Autosomal recessive spastic paraplegia type 74
- 2Early-onset X-linked optic atrophy
Showing 25 of 30. Retrieve the full set via the API.
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