359732009: Hereditary von Willebrand disease type 2N (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Functional finding\Disorder of hemostatic system\Blood coagulation disorder\von Willebrand disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 2\Hereditary von Willebrand disease type 2N (disorder)

\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 2\Hereditary von Willebrand disease type 2N (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hereditary von Willebrand disease type 2N (disorder)
\Disease\Disorder of hemostatic system\Blood coagulation disorder\von Willebrand disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 2\Hereditary von Willebrand disease type 2N (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

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

5156384013 Hereditary von Willebrand disease type 2N (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5156385014 Hereditary von Willebrand disease type 2N en Synonym (core metadata concept) Active Only initial character case insensitive (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 Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary von Willebrand disease type 2N (disorder)	Is a	von Willebrand disorder	false	Inferred relationship	Some
Hereditary von Willebrand disease type 2N (disorder)	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Some
Hereditary von Willebrand disease type 2N (disorder)	Finding site	Body system structure	false	Inferred relationship	Some
Hereditary von Willebrand disease type 2N (disorder)	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
Hereditary von Willebrand disease type 2N (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Hereditary von Willebrand disease type 2N (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Some	1
Hereditary von Willebrand disease type 2N (disorder)	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Hereditary von Willebrand disease type 2N (disorder)	Is a	Hereditary von Willebrand disease type 2	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
von Willebrand Normandy screening test (procedure)	Has focus	True	Hereditary von Willebrand disease type 2N (disorder)	Inferred relationship	Some	2

This concept is not in any reference sets