OMOP Concept 35623403
Autosomal dominant intermediate Charcot-Marie-Tooth disease type A
StandardConditionSNOMED765744006Disorder
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 Autosomal dominant intermediate Charcot-Marie-Tooth disease type A via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C564702 | Charcot-Marie-Tooth Disease, Dominant Intermediate A | Non-standard |
| Nebraska Lexicon | 765744006 | Autosomal dominant intermediate Charcot-Marie-Tooth disease type A | Non-standard |
Synonyms
Alternative names recorded for Autosomal dominant intermediate Charcot-Marie-Tooth disease type A across source vocabularies.
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type A (disorder)
- enfermedad de Charcot-Marie-Tooth autosómica dominante tipo A
- enfermedad de Charcot-Marie-Tooth autosómica dominante tipo A (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(13)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Hereditary motor and sensory neuropathy
- 2Autosomal hereditary disorder
- 2Hereditary peripheral neuropathy
- 3Disorder of the peripheral nervous system
- 3Hereditary disease
- 3Hereditary disorder of nervous system
- 4Disorder of nervous system
- 4Genetic disease
- 4Hereditary disorder by system
- 5Disease
- 5Disorder of body system
- 6Clinical finding
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