128113003: von Willebrand disease type IB (disorder)

• SNOMED CT Concept\constatation clinique\...
• \constatation fonctionnelle\Disorder of haemostatic system\Blood coagulation disorder\maladie de von Willebrand\von Willebrand disease type 1\von Willebrand disease type IB
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\von Willebrand disease type 1\von Willebrand disease type IB
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\maladie de von Willebrand\von Willebrand disease type 1\von Willebrand disease type IB

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
3891029013	Hereditary von Willebrand disease type 1B	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

Expanded Value Set

This concept is not in any reference sets

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