OMOP Concept 4027375
Scott syndrome
StandardConditionSNOMED128098009Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Scott syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C563120 | Scott Syndrome | Non-standard |
| Nebraska Lexicon | 128098009 | Scott syndrome | Non-standard |
Synonyms
Alternative names recorded for Scott syndrome across source vocabularies.
- Scott syndrome (disorder)
- síndrome de Scott
- síndrome de Scott (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(15)Roll up to these when you need a wider cohort.
- 1Hereditary platelet function disorder
- 2Inherited platelet disorder
- 2Qualitative platelet disorder
- 3Hereditary disorder of cellular element of blood
- 3Platelet disorder
- 4Disorder of cellular component of blood
- 4Disorder of hemostatic system
- 4Hereditary disorder by system
- 5Disease
- 5Disorder of body system
- 5Finding of blood, lymphatics and immune system
- 5Functional finding
- 5Hereditary disease
- 6Clinical finding
- 6Genetic disease
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