OMOP Concept 37166157
Hereditary von Willebrand disease
StandardConditionSNOMED1259242002Disorder
Maps from
2
Descendants
10
Valid from
30 Nov 2022
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Hereditary von Willebrand disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 155728 | Congenital Von Willebrand's disease | Non-standard |
| Nebraska Lexicon | 234446004 | Congenital von Willebrand disease | Non-standard |
Synonyms
Alternative names recorded for Hereditary von Willebrand disease across source vocabularies.
- enfermedad hereditaria de von Willebrand
- enfermedad hereditaria de von Willebrand (trastorno)
- Hereditary von Willebrand disease (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(11)Roll up to these when you need a wider cohort.
Narrower concepts
(10)Included automatically when you query with descendants.
- 1Hereditary von Willebrand disease type 1
- 1Hereditary von Willebrand disease type 2
- 1Hereditary von Willebrand disease type 3
- 2Hereditary von Willebrand disease type 1A
- 2Hereditary von Willebrand disease type 1B
- 2Hereditary von Willebrand disease type 1C
- 2Hereditary von Willebrand disease type 2A
- 2Hereditary von Willebrand disease type 2B
- 2Hereditary von Willebrand disease type 2M
- 2Hereditary von Willebrand disease type 2N
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