359711001: Hereditary von Willebrand disease type 2A (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 2A

\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 2\Hereditary von Willebrand disease type 2A
\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 2A

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

474818018 Hereditary von Willebrand disease type 2A en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

733587018 Hereditary von Willebrand disease type 2A (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5223581000241113 maladie de von Willebrand, type 2A, héréditaire fr Synonym (core metadata concept) Active Only initial character case insensitive (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 2A	Is a	von Willebrand disorder	false	Inferred relationship	Some
Hereditary von Willebrand disease type 2A	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Some
Hereditary von Willebrand disease type 2A	Finding site	Body system structure	false	Inferred relationship	Some
Hereditary von Willebrand disease type 2A	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
Hereditary von Willebrand disease type 2A	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Hereditary von Willebrand disease type 2A	Has interpretation	Abnormal	true	Inferred relationship	Some	1
Hereditary von Willebrand disease type 2A	Is a	Hereditary von Willebrand disease type 2	true	Inferred relationship	Some

Inbound Relationships

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Active

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Reference Sets