128115005: Pseudo von Willebrand disease (disorder)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

194709016 Pseudo von Willebrand disease en Synonym Active Initial character case insensitive SNOMED CT core

5156402014 Platelet type-von Willebrand disease en Synonym Active Initial character case insensitive SNOMED CT core

5156403016 Pseudo-von Willebrand disease type 2B en Synonym Active Initial character case insensitive SNOMED CT core

5156404010 PT-VWD - platelet type-von Willebrand disease en Synonym Active Case sensitive SNOMED CT core

5156406012 Platelet type pseudo-von Willebrand disease en Synonym Active Initial character case insensitive SNOMED CT core

732077016 Pseudo von Willebrand disease (disorder) en Fully specified name Active Initial character case insensitive 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 Case sensitive SNOMED CT core

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Pseudo von Willebrand disease	Interprets	Haemostatic 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	true	Inferred relationship	Some
Pseudo von Willebrand disease	Finding site	Body system structure	true	Inferred relationship	Some	2
Pseudo von Willebrand disease	Is a	Blood coagulation disorder	true	Inferred relationship	Some
Pseudo von Willebrand disease	Is a	Hereditary disorder of haematologic system	false	Inferred relationship	Some
Pseudo von Willebrand disease	Is a	Autosomal dominant hereditary disorder	true	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	Haemostatic system finding	false	Inferred relationship	Some
Pseudo von Willebrand disease	Finding site	Entire haematological system	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Id	Description	Lang	Type	Status	Case?	Module
194709016	Pseudo von Willebrand disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
5156402014	Platelet type-von Willebrand disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
5156403016	Pseudo-von Willebrand disease type 2B	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
5156404010	PT-VWD - platelet type-von Willebrand disease	en	Synonym	Active	Case sensitive	SNOMED CT core
5156406012	Platelet type pseudo-von Willebrand disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
732077016	Pseudo von Willebrand disease (disorder)	en	Fully specified name	Active	Initial character case insensitive	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	Case sensitive	SNOMED CT core