OMOP Concept 36717210
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
StandardConditionSNOMED722294004Disorder
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 intermediate Charcot-Marie-Tooth disease type E via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 722294004 | Autosomal dominant intermediate Charcot-Marie-Tooth disease type E | Non-standard |
Synonyms
Alternative names recorded for Autosomal dominant intermediate Charcot-Marie-Tooth disease type E across source vocabularies.
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type E (disorder)
- Charcot-Marie-Tooth disease with nephropathy syndrome
- enfermedad de Charcot-Marie-Tooth autosómica dominante tipo E
- enfermedad de Charcot-Marie-Tooth autosómica dominante tipo E (trastorno)
- síndrome de enfermedad de Charcot-Marie-Tooth con nefropatía
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(33)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Glomerular disease
- 1Hereditary motor and sensory neuropathy
- 1Hereditary nephropathy
- 2Autosomal hereditary disorder
- 2Disorder of renal parenchyma
- 2Hereditary disorder of the urinary system
- 2Hereditary peripheral neuropathy
- 2Kidney disease
- 3Disorder of kidney and/or ureter
- 3Disorder of retroperitoneum
- 3Disorder of the peripheral nervous system
- 3Disorder of urinary system
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Hereditary disorder of nervous system
- 3Kidney finding
- 4Abdominal organ finding
- 4Disorder of abdomen
- 4Disorder of body system
- 4Disorder of nervous system
- 4Disorder of the genitourinary system
- 4Genetic disease
- 4Urinary system finding
- 5Disease
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