OMOP Concept 4125643
Prothrombin complex deficiency
StandardConditionSNOMED234454002Disorder
Maps from
1
Descendants
11
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Prothrombin complex deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 234454002 | Prothrombin complex deficiency | Non-standard |
Synonyms
Alternative names recorded for Prothrombin complex deficiency across source vocabularies.
- deficiencia del complejo protrombina
- deficiencia del complejo protrombina (trastorno)
- Prothrombin complex deficiency (disorder)
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
(11)Included automatically when you query with descendants.
- 1Factor II deficiency
- 1Factor VII deficiency
- 1Factor X deficiency
- 2Acquired factor II deficiency
- 2Acquired factor VII deficiency disease
- 2Acquired factor X deficiency disease
- 2Factor X deficiency due to systemic amyloidosis
- 2Hereditary factor II deficiency disease
- 2Hereditary factor VII deficiency disease
- 2Hereditary factor X deficiency disease
- 3Prothrombin 2 mutation with hypercoagulability
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