OMOP Concept 4133987
Hereditary von Willebrand disease type 1B
StandardConditionSNOMED128113003Disorder
Maps from
1
Descendants
0
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 Hereditary von Willebrand disease type 1B via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 128113003 | von Willebrand disease type IB | Non-standard |
Synonyms
Alternative names recorded for Hereditary von Willebrand disease type 1B across source vocabularies.
- enfermedad de von Willebrand hereditaria tipo 1B
- enfermedad de von Willebrand hereditaria tipo 1B (trastorno)
- enfermedad de von Willebrand hereditaria tipo IB
- Hereditary von Willebrand disease type 1B (disorder)
- Hereditary von Willebrand disease type IB
- von Willebrand disease type IB
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(14)Roll up to these when you need a wider cohort.
- 1Hereditary von Willebrand disease type 1
- 2Autosomal dominant hereditary disorder
- 2Hereditary von Willebrand disease
- 3Autosomal hereditary disorder
- 3von Willebrand disorder
- 4Blood coagulation disorder
- 4Hereditary disease
- 5Disorder of hemostatic system
- 5Genetic disease
- 5OMOP Bleeding 1
- 5OMOP Bleeding 2
- 6Disease
- 6Functional finding
- 7Clinical finding
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