359711001: Hereditary von Willebrand disease type 2A (disorder)

• SNOMED CT Concept\constatation clinique\...
• \constatation fonctionnelle\Disorder of haemostatic system\Blood coagulation disorder\maladie de von Willebrand\von Willebrand disease type 2\Hereditary von Willebrand disease type 2A
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\von Willebrand disease type 2\Hereditary von Willebrand disease type 2A
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\maladie de von Willebrand\von Willebrand disease type 2\Hereditary von Willebrand disease type 2A

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
733587018	Hereditary von Willebrand disease type 2A (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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