OMOP Concept 37204322
Gastrocutaneous syndrome
StandardConditionSNOMED782946000Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2019
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Gastrocutaneous syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535651 | Gastrocutaneous syndrome | Non-standard |
Synonyms
Alternative names recorded for Gastrocutaneous syndrome across source vocabularies.
- Gastrocutaneous syndrome (disorder)
- síndrome gastrocutáneo
- síndrome gastrocutáneo (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(34)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Digestive system hereditary disorder
- 1Disorder of upper gastrointestinal tract
- 1Genetic disorder of skin pigmentation
- 1Hereditary disorder of the integument
- 1Hyperpigmentation of skin
- 2Autosomal hereditary disorder
- 2Disorder of digestive system
- 2Disorder of gastrointestinal tract
- 2Disorder of integument
- 2Disorder of skin pigmentation
- 2Disorder of upper digestive tract
- 2Genetic disease
- 2Hereditary disorder by system
- 2Skin deposits
- 3Digestive system finding
- 3Disease
- 3Disorder of body system
- 3Disorder of digestive tract
- 3Disorder of pigmentation
- 3Disorder of skin
- 3Gastrointestinal tract finding
- 3Hereditary disease
- 3Integumentary system finding
- 3Skin lesion
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