OMOP Concept 4227574
Factor XI deficiency, type I
StandardConditionSNOMED88540000Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Factor XI deficiency, type I via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 140799 | Factor XI deficiency, type I | Non-standard |
| Nebraska Lexicon | 88540000 | Factor XI deficiency, type I | Non-standard |
Synonyms
Alternative names recorded for Factor XI deficiency, type I across source vocabularies.
- deficiencia de factor XI, tipo I
- deficiencia de factor XI, tipo I (trastorno)
- Factor XI deficiency, type I (disorder)
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.
- 1Hereditary factor XI deficiency disease
- 2Autosomal recessive hereditary disorder
- 2Congenital disease
- 2Contact factor deficiency
- 2Factor XI deficiency
- 2Hemophilia
- 3Autosomal hereditary disorder
- 3Blood coagulation disorder
- 3Coagulation factor deficiency syndrome
- 3Disorder of fetus and/or newborn
- 4Disease
- 4Disorder of hemostatic system
- 4Hereditary disease
- 4OMOP Bleeding 1
- 4OMOP Bleeding 2
- 5Clinical finding
- 5Functional finding
- 5Genetic disease
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