OMOP Concept 35622280
Lichtenstein syndrome
StandardConditionSNOMED763668009Disorder
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 Lichtenstein syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535894 | Lichtenstein syndrome | Non-standard |
| Nebraska Lexicon | 763668009 | Lichtenstein syndrome | Non-standard |
Synonyms
Alternative names recorded for Lichtenstein syndrome across source vocabularies.
- Lichtenstein syndrome (disorder)
- síndrome de Lichtenstein
- síndrome de Lichtenstein (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(18)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital immunodeficiency disease
- 1Disorder of immune structure
- 1Hereditary disorder of immune system
- 1Phagocytic cell dysfunction
- 2Autosomal hereditary disorder
- 2Congenital disease
- 2Disorder of body system
- 2Disorder of immune function
- 2Hereditary disorder by system
- 2Immunodeficiency disorder
- 2Phagocytic cell defect
- 3Disease
- 3Disorder of fetus and/or newborn
- 3Hereditary disease
- 3Primary immune deficiency disorder
- 4Clinical finding
- 4Genetic disease
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