128108002: Hereditary von Willebrand disease type 3 (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of hemostatic system\Blood coagulation disorder\von Willebrand disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 3
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 3
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hereditary von Willebrand disease type 3
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\von Willebrand disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 3

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
194702013	von Willebrand disease type 3	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
206398017	Hereditary von Willebrand disease type 3	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
732069015	von Willebrand disease type 3 (disorder)	en	Fully specified name	Inactive	Entire term case sensitive	SNOMED CT core module
5034731017	von Willebrand disease type III	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
5156393014	Hereditary von Willebrand disease type 3 (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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