128114009: Hereditary von Willebrand disease type 1C (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of hemostatic system\Blood coagulation disorder\von Willebrand disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 1\Hereditary von Willebrand disease type 1C
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 1\Hereditary von Willebrand disease type 1C
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary von Willebrand disease type 1\Hereditary von Willebrand disease type 1C
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\von Willebrand disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 1\Hereditary von Willebrand disease type 1C

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
194708012	von Willebrand disease type IC	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
206400018	Hereditary von Willebrand disease type IC	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3891027010	Hereditary von Willebrand disease type 1C	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
5156379019	Hereditary von Willebrand disease type 1C (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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