234446004: Congenital von Willebrand's disease (disorder)

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

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
110611000077117	maladie de von Willebrand congénitale	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
2839593011	Congenital von Willebrand disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
351268018	Congenital von Willebrand's disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
351269014	vWD - Congenital von Willebrand's disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
382281000077119	maladie de von Willebrand congénitale (trouble)	fr	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
622765010	Congenital von Willebrand's disease (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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