359732009: von Willebrand disease type 2N (disorder)

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

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

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

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

1944991000052116 von Willebrands sjukdom, typ 2N sv Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

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

This concept is not in any reference sets