359732009: von Willebrand disease type 2N (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation fonctionnelle\Disorder of haemostatic system\Blood coagulation disorder\maladie de von Willebrand\von Willebrand disease type 2\von Willebrand disease type 2N

\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\von Willebrand disease type 2\von Willebrand disease type 2N
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\von Willebrand disease type 2N
\Disease\Disorder of haemostatic system\Blood coagulation disorder\maladie de von Willebrand\von Willebrand disease type 2\von Willebrand disease type 2N

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

474895016 von Willebrand disease type 2N en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

609141000241119 maladie de von Willebrand type 2N (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

734275018 von Willebrand disease type 2N (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

892871000172111 maladie de von Willebrand type 2N fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
von Willebrand disease type 2N	interprète (attribut)	Hemostatic function (observable entity)	true	Inferred relationship	Some	1
von Willebrand disease type 2N	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	1
von Willebrand disease type 2N	est un(e) (attribut)	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
von Willebrand disease type 2N	est un(e) (attribut)	von Willebrand disease type 2	true	Inferred relationship	Some
von Willebrand disease type 2N	est un(e) (attribut)	maladie de von Willebrand	false	Inferred relationship	Some
von Willebrand disease type 2N	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
von Willebrand disease type 2N	est défini par la manifestation de (attribut)	constatation sur le système hémostatique	false	Inferred relationship	Some
von Willebrand disease type 2N	localisation d'une constatation (attribut)	Entire hematological system (body structure)	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
von Willebrand Normandy screening test (procedure)	a pour objet (attribut)	True	von Willebrand disease type 2N	Inferred relationship	Some	2

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)