OMOP Concept 4320820
Disorder involving the fibrinolytic system
StandardConditionSNOMED95839005Disorder
Maps from
2
Descendants
17
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 Disorder involving the fibrinolytic system via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 142136 | Disorder involving the fibrinolytic system | Non-standard |
| CIEL | 169899 | Inherited fibrinolytic defect | Non-standard |
Synonyms
Alternative names recorded for Disorder involving the fibrinolytic system across source vocabularies.
- Disorder involving the fibrinolytic system (disorder)
- Disorder of fibrinolysis
- trastorno de la fibrinólisis
- trastorno que compromete el sistema fibrinolítico
- trastorno que compromete el sistema fibrinolítico (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(7)Roll up to these when you need a wider cohort.
Narrower concepts
(17)Included automatically when you query with descendants.
- 1Drug-induced fibrinolytic disorder
- 1Dysplasminogenemia
- 1Fibrinolytic bleeding syndrome
- 1Fibrinolytic disorder caused by tissue plasminogen activator
- 1Hyperfibrinolysis
- 1Postpartum disorder of abnormal fibrinolysis
- 1Systemic fibrinogenolysis
- 2Alpha-2-antiplasmin deficiency
- 2Antepartum hemorrhage with hyperfibrinolysis
- 2Fibrinolytic disorder caused by urokinase
- 2Hereditary dysplasminogenemia
- 2Hypoplasminogenemia
- 2Postpartum fibrinolysis with hemorrhage
- 3Acquired hypoplasminogenemia
- 3Congenital alpha-2-antiplasmin deficiency
- 3Hereditary hypoplasminogenemia
- 4Autosomal dominant deficiency of plasminogen
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