OMOP Concept 4290771
Hereditary factor X deficiency disease
StandardConditionSNOMED37350004Disorder
Maps from
2
Descendants
0
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 Hereditary factor X deficiency disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138774 | Hereditary factor X deficiency disease | Non-standard |
| Nebraska Lexicon | 37350004 | Hereditary Stuart-Prower deficiency disease | Non-standard |
Synonyms
Alternative names recorded for Hereditary factor X deficiency disease across source vocabularies.
- deficiencia hereditaria de factor de Stuart
- deficiencia hereditaria de factor X
- deficiencia hereditaria de factor X (trastorno)
- deficiencia hereditaria de Stuart - Prower
- Hereditary factor X deficiency disease (disorder)
- Hereditary Stuart factor deficiency disease
- Hereditary Stuart-Prower deficiency disease
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
- 1Factor X deficiency
- 1Hereditary coagulation factor deficiency
- 2Autosomal hereditary disorder
- 2Coagulation factor deficiency syndrome
- 2Hereditary disease
- 2Prothrombin complex deficiency
- 3Blood coagulation disorder
- 3Genetic disease
- 4Disease
- 4Disorder of hemostatic system
- 4OMOP Bleeding 1
- 4OMOP Bleeding 2
- 5Clinical finding
- 5Functional finding
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