OMOP Concept 4234868
Hereditary von Willebrand disease type 2A
StandardConditionSNOMED359711001Disorder
Maps from
5
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
5 source codes normalize to Hereditary von Willebrand disease type 2A via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 122976 | Von Willebrand disease, type IIa | Non-standard |
| ICD10CM | D68.020 | Von Willebrand disease, type 2A | Non-standard |
| Nebraska Lexicon | 359711001 | Hereditary von Willebrand disease type 2A | Non-standard |
| Nebraska Lexicon | 359714009 | von Willebrand disease type 2A | Non-standard |
| Nebraska Lexicon | 87397002 | von Willebrand disease, type IIA | Non-standard |
Synonyms
Alternative names recorded for Hereditary von Willebrand disease type 2A across source vocabularies.
- enfermedad de von Willebrand hereditaria tipo 2A
- enfermedad de von Willebrand hereditaria tipo 2A (trastorno)
- Hereditary von Willebrand disease type 2A (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(13)Roll up to these when you need a wider cohort.
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