OMOP Concept 35622281
Spastic ataxia with congenital miosis
StandardConditionSNOMED763669001Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2018
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Spastic ataxia with congenital miosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C566247 | Ataxia, Spastic, with Congenital Miosis | Non-standard |
| Nebraska Lexicon | 763669001 | Autosomal dominant spastic ataxia type 7 | Non-standard |
Synonyms
Alternative names recorded for Spastic ataxia with congenital miosis across source vocabularies.
- ataxia espástica autosómica dominante tipo 7
- ataxia espástica con miosis congénita
- ataxia espástica con miosis congénita (trastorno)
- Autosomal dominant spastic ataxia type 7
- Spastic ataxia with congenital miosis (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(42)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital miosis
- 1Developmental hereditary disorder
- 1Disorder of the central nervous system
- 1Hereditary ataxia
- 1Hereditary disorder of the visual system
- 2Ataxia
- 2Autosomal hereditary disorder
- 2Central nervous system finding
- 2Congenital anomaly of pupil
- 2Constricted pupil
- 2Developmental disorder
- 2Disorder of nervous system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Hereditary disorder of nervous system
- 2Visual system disorder
- 3Clinical finding
- 3Congenital anomaly of eye
- 3Disease
- 3Disorder of body system
- 3Eye / vision finding
- 3Finding of size of pupil
- 3Finding related to coordination / incoordination
- 3Functional finding
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