234447008: Congenital von Willebrand's disease type I (disorder)

• SNOMED CT Concept\constatation clinique\...
• \constatation fonctionnelle\Disorder of haemostatic system\Blood coagulation disorder\maladie de von Willebrand\maladie de von Willebrand congénitale\Congenital von Willebrand's disease type I
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\maladie de von Willebrand\maladie de von Willebrand congénitale\Congenital von Willebrand's disease type I
• \Disease\Congenital disease\maladie de von Willebrand congénitale\Congenital von Willebrand's disease type I

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
2841830016	Congenital von Willebrand disease type I	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
351270010	vWD - Congenital von Willebrand's disease type I	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
351271014	Congenital von Willebrand's disease type I	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
622766011	Congenital von Willebrand's disease type I (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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