359700009: Hereditary von Willebrand disease type 1A (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 1\Hereditary von Willebrand disease type 1A
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 1\Hereditary von Willebrand disease type 1A
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary von Willebrand disease type 1\Hereditary von Willebrand disease type 1A
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\von Willebrand disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 1\Hereditary von Willebrand disease type 1A

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
474740015	Hereditary von Willebrand disease type IA	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3891028017	Hereditary von Willebrand disease type 1A	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
5156374012	Hereditary von Willebrand disease type 1A (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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