234473003: Platelet type von Willebrand's disease (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of blood, lymphatics and immune system\Blood disease\...
• \Hereditary disorder of cellular element of blood\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ib defect\Platelet type von Willebrand's disease
• \Platelet disorder\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ib defect\Platelet type von Willebrand's disease
• \Functional finding\Disorder of haemostatic system\Platelet disorder\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ib defect\Platelet type von Willebrand's disease
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ib defect\Platelet type von Willebrand's disease
• \Disease\Blood disease\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ib defect\Platelet type von Willebrand's disease
• \Disease\Blood disease\Platelet disorder\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ib defect\Platelet type von Willebrand's disease
• \Disease\Disorder of haemostatic system\Platelet disorder\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ib defect\Platelet type von Willebrand's disease
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ib defect\Platelet type von Willebrand's disease

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2839594017	Platelet type von Willebrand disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
351306019	Platelet type von Willebrand's disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
622798017	Platelet type von Willebrand's disease (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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