359725000: Hereditary von Willebrand disease type 2M (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of haemostatic system\Blood coagulation disorder\von Willebrand disorder\Hereditary von Willebrand disease\von Willebrand disease type 2\Hereditary von Willebrand disease type 2M
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hereditary von Willebrand disease\von Willebrand disease type 2\Hereditary von Willebrand disease type 2M
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary von Willebrand disease type 2M
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\von Willebrand disorder\Hereditary von Willebrand disease\von Willebrand disease type 2\Hereditary von Willebrand disease type 2M

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
474870017	Hereditary von Willebrand disease type 2M	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
734045018	Hereditary von Willebrand disease type 2M (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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