128113003: Hereditary von Willebrand disease type 1B (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 1B
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 1\Hereditary von Willebrand disease type 1B
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary von Willebrand disease type 1\Hereditary von Willebrand disease type 1B
• \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 1B

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
194707019	von Willebrand disease type IB	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
206399013	Hereditary von Willebrand disease type IB	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
732075012	von Willebrand disease type IB (disorder)	en	Fully specified name	Inactive	Entire term case sensitive	SNOMED CT core module
3891029013	Hereditary von Willebrand disease type 1B	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
5156378010	Hereditary von Willebrand disease type 1B (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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