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

SNOMED CT Concept\Clinical finding (finding)\...

\Functional finding\Disorder of hemostatic 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 (disorder)\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ib defect\Platelet type von Willebrand's disease
\Disease\Disorder of cellular component of blood (disorder)\Hereditary disorder of cellular element of blood (disorder)\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ib defect\Platelet type von Willebrand's disease
\Disease\Disorder of cellular component of blood (disorder)\Platelet disorder\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ib defect\Platelet type von Willebrand's disease
\Disease\Disorder of hemostatic 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 (disorder)\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ib defect\Platelet type von Willebrand's disease

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

351306019 Platelet type von Willebrand's disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

622798017 Platelet type von Willebrand's disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2839594017 Platelet type von Willebrand disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3367271000052114 von Willebrands sjukdom av trombocyttyp sv Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Platelet type von Willebrand's disease	Is a	Glycoprotein Ib defect	true	Inferred relationship	Some
Platelet type von Willebrand's disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Platelet type von Willebrand's disease	Finding site	Platelet	false	Inferred relationship	Some
Platelet type von Willebrand's disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Platelet type von Willebrand's disease	Finding site	Body system structure	false	Inferred relationship	Some
Platelet type von Willebrand's disease	Has definitional manifestation	Platelet finding	false	Inferred relationship	Some
Platelet type von Willebrand's disease	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
Platelet type von Willebrand's disease	Finding site	Body system structure	true	Inferred relationship	Some	2
Platelet type von Willebrand's disease	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Platelet type von Willebrand's disease	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

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Group

This concept is not in any reference sets