359711001: Hereditary von Willebrand disease type 2A (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 2A
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hereditary von Willebrand disease\von Willebrand disease type 2\Hereditary von Willebrand disease type 2A
• \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 2A

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
474818018	Hereditary von Willebrand disease type 2A	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
733587018	Hereditary von Willebrand disease type 2A (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

Australian dialect reference set

Problem/Diagnosis reference set

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