OMOP Concept 4234870
Hereditary von Willebrand disease type 2N
StandardConditionSNOMED359732009Disorder
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 von Willebrand disease type 2N via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| ICD10CM | D68.023 | Von Willebrand disease, type 2N | Non-standard |
| Nebraska Lexicon | 359732009 | von Willebrand disease type 2N | Non-standard |
Synonyms
Alternative names recorded for Hereditary von Willebrand disease type 2N across source vocabularies.
- enfermedad de von Willebrand hereditaria tipo 2N
- enfermedad de von Willebrand hereditaria tipo 2N (trastorno)
- enfermedad de von Willebrand tipo 2N
- Hereditary von Willebrand disease type 2N (disorder)
- von Willebrand disease type 2N
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.
- 1Autosomal recessive hereditary disorder
- 1Hereditary von Willebrand disease type 2
- 2Autosomal hereditary disorder
- 2Hereditary von Willebrand disease
- 3Hereditary disease
- 3von Willebrand disorder
- 4Blood coagulation disorder
- 4Genetic disease
- 5Disease
- 5Disorder of hemostatic system
- 5OMOP Bleeding 1
- 5OMOP Bleeding 2
- 6Clinical finding
- 6Functional finding
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