128106003: Hereditary von Willebrand disease type 1 (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 1
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hereditary von Willebrand disease\von Willebrand disease type 1
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\von Willebrand disease type 1
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\von Willebrand disorder\Hereditary von Willebrand disease\von Willebrand disease type 1

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
194700017	von Willebrand disease type 1	en	Synonym	Active	Case sensitive	SNOMED CT core
206396018	Hereditary von Willebrand disease type 1	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
5156373018	Hereditary von Willebrand disease type 1 (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
732067018	von Willebrand disease type 1 (disorder)	en	Fully specified name	Inactive	Case sensitive	SNOMED CT core
5156372011	A form of von Willebrand disease (VWD) with characteristics of a bleeding disorder associated with a partial, quantitative plasmatic deficiency of an otherwise structurally and functionally normal von Willebrand factor (VWF). The type 1 disease is considered to be the most common form of VWD, caused by mutations in the VWF gene (12p13.3). Transmitted in an autosomal dominant manner.	en	Definition	Active	Case sensitive	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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