OMOP Concept 36717089
Autosomal dominant Charcot-Marie-Tooth disease type 2L
StandardConditionSNOMED719513008Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Autosomal dominant Charcot-Marie-Tooth disease type 2L via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 719513008 | Autosomal dominant Charcot-Marie-Tooth disease type 2L | Non-standard |
Synonyms
Alternative names recorded for Autosomal dominant Charcot-Marie-Tooth disease type 2L across source vocabularies.
- Autosomal dominant Charcot-Marie-Tooth disease type 2L (disorder)
- enfermedad de Charcot-Marie-Tooth tipo 2L autosómica dominante
- enfermedad de Charcot-Marie-Tooth tipo 2L autosómica dominante (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(17)Roll up to these when you need a wider cohort.
- 1Autosomal dominant Charcot-Marie-Tooth disease type 2
- 2Autosomal dominant hereditary disorder
- 2Charcot-Marie-Tooth disease, type II
- 3Autosomal hereditary disorder
- 3Degenerative disorder
- 3Hereditary motor and sensory neuropathy
- 3Neuropathy
- 4Disease
- 4Disorder of nervous system
- 4Hereditary disease
- 4Hereditary peripheral neuropathy
- 5Clinical finding
- 5Disorder of body system
- 5Disorder of the peripheral nervous system
- 5Genetic disease
- 5Hereditary disorder of nervous system
- 6Hereditary disorder by system
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