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 (disorder)\...

\Hereditary disorder of cellular element of blood (disorder)\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\...

\Blood coagulation 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

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\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 (disorder)\Hereditary disorder of cellular element of blood (disorder)\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Pseudo von Willebrand disease
\Disease\Disorder of cellular component of blood (disorder)\Platelet disorder\Qualitative platelet disorder (disorder)\Hereditary platelet function disorder (disorder)\Pseudo von Willebrand disease
\Disease\Disorder of cellular component of blood (disorder)\Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Pseudo von Willebrand disease
\Disease\Disorder of hemostatic system\Blood coagulation disorder\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\Hereditary disorder of cellular element of blood (disorder)\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:

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
2884480017 Any inherited disorder mimicking von Willebrand disease but lacking mutation at the VWF locus en Definition Inactive 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

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Pseudo von Willebrand disease	Is a	Blood coagulation disorder	true	Inferred relationship	Some
Pseudo von Willebrand disease	Is a	Hereditary disorder of hematologic system	false	Inferred relationship	Some
Pseudo von Willebrand disease	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Pseudo von Willebrand disease	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Some
Pseudo von Willebrand disease	Is a	Hereditary disorder by system	false	Inferred relationship	Some
Pseudo von Willebrand disease	Finding site	Body system structure	false	Inferred relationship	Some
Pseudo von Willebrand disease	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
Pseudo von Willebrand disease	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Pseudo von Willebrand disease	Has interpretation	Abnormal	true	Inferred relationship	Some	1
Pseudo von Willebrand disease	Is a	Hereditary platelet function disorder (disorder)	true	Inferred relationship	Some
Pseudo von Willebrand disease	Finding site	Body system structure	true	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

GB English

US English

Back to Start

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
2884480017	Any inherited disorder mimicking von Willebrand disease but lacking mutation at the VWF locus	en	Definition	Inactive	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