359717002: Hereditary von Willebrand disease type 2B (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of haemostatic system\Blood coagulation disorder\von Willebrand disorder\Hereditary von Willebrand disease\von Willebrand disease type 2\Hereditary von Willebrand disease type 2B
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hereditary von Willebrand disease\von Willebrand disease type 2\Hereditary von Willebrand disease type 2B
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary von Willebrand disease type 2B
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\von Willebrand disorder\Hereditary von Willebrand disease\von Willebrand disease type 2\Hereditary von Willebrand disease type 2B

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
474846016	Hereditary von Willebrand disease type 2B	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
733815010	Hereditary von Willebrand disease type 2B (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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