OMOP Concept 4266973
Turcot syndrome
StandardConditionSNOMED61665008Disorder
Maps from
3
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
3 source codes normalize to Turcot syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 111782 | Turcot's syndrome | Non-standard |
| MeSH | C536928 | Turcot syndrome | Non-standard |
| Nebraska Lexicon | 61665008 | Turcot's syndrome | Non-standard |
Synonyms
Alternative names recorded for Turcot syndrome across source vocabularies.
- síndrome de Turcot
- síndrome de Turcot (trastorno)
- Turcot's syndrome
- Turcot syndrome (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(41)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Developmental hereditary disorder
- 1Familial multiple polyposis syndrome
- 2Autosomal hereditary disorder
- 2Developmental disorder
- 2Digestive system hereditary disorder
- 2Hereditary cancer-predisposing syndrome
- 2Hereditary disease
- 2Intestinal polyposis syndrome
- 2Polyp of large intestine
- 3Disease
- 3Disorder of digestive system
- 3Disorder of large intestine
- 3Genetic disease
- 3Hereditary disorder by system
- 3Polyp of intestine
- 4Abdominal mass
- 4Clinical finding
- 4Digestive system finding
- 4Disorder of body system
- 4Disorder of intestine
- 4Disorder of lower gastrointestinal tract
- 4Finding of large intestine
- 4Mass of digestive structure
- 4Polyp
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