OMOP Concept 37397281
Congenital plasminogen activator inhibitor deficiency type 1
StandardConditionSNOMED717407006Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Congenital plasminogen activator inhibitor deficiency type 1 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 717407006 | Congenital plasminogen activator inhibitor deficiency type 1 | Non-standard |
Synonyms
Alternative names recorded for Congenital plasminogen activator inhibitor deficiency type 1 across source vocabularies.
- Congenital plasminogen activator inhibitor deficiency type 1 (disorder)
- deficiencia congénita de inhibidor del activador del plasminógeno tipo 1
- deficiencia congénita de inhibidor del activador del plasminógeno tipo 1 (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.
- 1Autosomal recessive hereditary disorder
- 1Congenital disease
- 1Hereditary coagulation factor deficiency
- 2Autosomal hereditary disorder
- 2Coagulation factor deficiency syndrome
- 2Disorder of fetus and/or newborn
- 2Hereditary disease
- 3Blood coagulation disorder
- 3Disease
- 3Genetic disease
- 4Clinical finding
- 4Disorder of hemostatic system
- 4OMOP Bleeding 1
- 4OMOP Bleeding 2
- 5Functional finding
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