OMOP Concept 4027380

Hereditary von Willebrand disease type 2

StandardConditionSNOMED128107007Disorder
Maps from
9
Descendants
4
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept

9 source codes normalize to Hereditary von Willebrand disease type 2 via the OMOP "Maps to" relationship.

VocabularyCodeNameType
CIEL122969Von Willebrand disease, type IIhNon-standard
CIEL122970Von Willebrand disease, type IIgNon-standard
CIEL122971Von Willebrand disease, type IIfNon-standard
CIEL122972Von Willebrand disease, type IIeNon-standard
CIEL122973Von Willebrand disease, type IIdNon-standard
CIEL122974Von Willebrand disease, type IIcNon-standard
ICD10CMD68.02Von Willebrand disease, type 2Non-standard
ICD10CMD68.029Von Willebrand disease, type 2, unspecifiedNon-standard
MeSHD056728von Willebrand Disease, Type 2Non-standard

Synonyms

Alternative names recorded for Hereditary von Willebrand disease type 2 across source vocabularies.

  • enfermedad de von Willebrand hereditaria tipo 2
  • enfermedad de von Willebrand hereditaria tipo 2 (trastorno)
  • enfermedad de von Willebrand tipo 2
  • Hereditary von Willebrand disease type 2 (disorder)
  • von Willebrand disease type 2

Where it sits in the hierarchy

Ordered by distance - 1 is a direct parent or child.

Broader concepts

(12)

Roll up to these when you need a wider cohort.

Narrower concepts

(4)

Included automatically when you query with descendants.

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