359717002: Hereditary von Willebrand disease type 2B (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 2B
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\von Willebrand disease type 2\Hereditary von Willebrand disease type 2B
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary von Willebrand disease type 2B
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\maladie de von Willebrand\von Willebrand disease type 2\Hereditary von Willebrand disease type 2B

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
474846016	Hereditary von Willebrand disease type 2B	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
733815010	Hereditary von Willebrand disease type 2B (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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