88776002: Hereditary factor V deficiency disease (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\...
• \Hereditary coagulation factor deficiency\Hereditary factor V deficiency disease
• \Factor V deficiency\Hereditary factor V deficiency disease
• \Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor V deficiency disease
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor V deficiency disease
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor V deficiency\Hereditary factor V deficiency disease

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
147188010	Hereditary factor V deficiency disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
147189019	Parahemophilia	en	Synonym	Active	Case insensitive	SNOMED CT core
147190011	Hereditary hypoproaccelerinemia	en	Synonym	Active	Case insensitive	SNOMED CT core
147191010	Owren's disease	en	Synonym	Active	Case sensitive	SNOMED CT core
147193013	AC globulin deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
508192014	Parahaemophilia	en	Synonym	Active	Case insensitive	SNOMED CT core
508193016	Hereditary hypoproaccelerinaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
831530017	Hereditary factor V deficiency disease (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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