128113003: von Willebrand disease type IB (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Functional finding\Disorder of hemostatic system\Blood coagulation disorder\von Willebrand disorder\von Willebrand disease type 1 (disorder)\von Willebrand disease type IB (disorder)
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\von Willebrand disease type 1 (disorder)\von Willebrand disease type IB (disorder)
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\von Willebrand disorder\von Willebrand disease type 1 (disorder)\von Willebrand disease type IB (disorder)

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
194707019	von Willebrand disease type IB	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
206399013	Hereditary von Willebrand disease type IB	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
732075012	von Willebrand disease type IB (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3891029013	Hereditary von Willebrand disease type 1B	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1944811000052118	von Willebrands sjukdom, typ 1B	sv	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

This concept is not in any reference sets

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