128115005: Pseudo von Willebrand disease (disorder)

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

\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood\...

\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Pseudo von Willebrand disease

\Platelet disorder\Qualitative platelet disorder (disorder)\Hereditary platelet function disorder (disorder)\Pseudo von Willebrand disease
\Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Pseudo von Willebrand disease

\Functional finding\Disorder of hemostatic system\...

\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Pseudo von Willebrand disease

\Platelet disorder\Qualitative platelet disorder (disorder)\Hereditary platelet function disorder (disorder)\Pseudo von Willebrand disease
\Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Pseudo von Willebrand disease

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Pseudo von Willebrand disease
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Pseudo von Willebrand disease
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Pseudo von Willebrand disease
\Disease\Disorder of cellular component of blood\Platelet disorder\Qualitative platelet disorder (disorder)\Hereditary platelet function disorder (disorder)\Pseudo von Willebrand disease
\Disease\Disorder of cellular component of blood\Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Pseudo von Willebrand disease
\Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Pseudo von Willebrand disease
\Disease\Disorder of hemostatic system\Platelet disorder\Qualitative platelet disorder (disorder)\Hereditary platelet function disorder (disorder)\Pseudo von Willebrand disease
\Disease\Disorder of hemostatic system\Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Pseudo von Willebrand disease
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Pseudo von Willebrand disease

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Pseudo von Willebrand disease	Is a	Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudo von Willebrand disease	Is a	Hereditary disorder of haematologic sysem	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudo von Willebrand disease	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudo von Willebrand disease	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudo von Willebrand disease	Is a	Hereditary disorder by system (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudo von Willebrand disease	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudo von Willebrand disease	Has definitional manifestation	Hemostatic system finding (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudo von Willebrand disease	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pseudo von Willebrand disease	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pseudo von Willebrand disease	Is a	Hereditary platelet function disorder (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudo von Willebrand disease	Finding site	Body system structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

GB English

US English

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Id	Description	Lang	Type	Status	Case?	Module
194709016	Pseudo von Willebrand disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
732077016	Pseudo von Willebrand disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5156402014	Platelet type-von Willebrand disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5156403016	Pseudo-von Willebrand disease type 2B	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5156404010	PT-VWD - platelet type-von Willebrand disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5156406012	Platelet type pseudo-von Willebrand disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5156405011	A bleeding disorder with characteristics of mild to moderate mucocutaneous bleeding, which becomes more pronounced during pregnancy or following ingestion of drugs that have anti-platelet activity. This disease is due to hyperresponsive platelets, resulting in thrombocytopenia.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
194709016	Pseudo von Willebrand disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
732077016	Pseudo von Willebrand disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5156402014	Platelet type-von Willebrand disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5156403016	Pseudo-von Willebrand disease type 2B	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5156404010	PT-VWD - platelet type-von Willebrand disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5156406012	Platelet type pseudo-von Willebrand disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2884480017	Any inherited disorder mimicking von Willebrand disease but lacking mutation at the VWF locus	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5156405011	A bleeding disorder with characteristics of mild to moderate mucocutaneous bleeding, which becomes more pronounced during pregnancy or following ingestion of drugs that have anti-platelet activity. This disease is due to hyperresponsive platelets, resulting in thrombocytopenia.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3410131001000118	Pseudo-von-Willebrand-Syndrom	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
888121000172117	maladie de von Willebrand type plaquette	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
941431000172118	PT-VWD - platelet type-von Willebrand disease	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
888121000172117	maladie de von Willebrand type plaquette	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
941431000172118	PT-VWD - platelet type-von Willebrand disease	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3410131001000118	Pseudo-von-Willebrand-Syndrom	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module