359700009: Hereditary von Willebrand disease type IA (disorder)

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

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
474740015	Hereditary von Willebrand disease type IA	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
733243011	Hereditary von Willebrand disease type IA (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3891028017	Hereditary von Willebrand disease type 1A	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1953371000052115	ärftlig von Willebrands sjukdom, typ 1A	sv	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

This concept is not in any reference sets

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