359725000: Hereditary von Willebrand disease type 2M (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 2\Hereditary von Willebrand disease type 2M
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 2\Hereditary von Willebrand disease type 2M
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary von Willebrand disease type 2M
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\von Willebrand disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 2\Hereditary von Willebrand disease type 2M

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
474870017	Hereditary von Willebrand disease type 2M	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
734045018	Hereditary von Willebrand disease type 2M (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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