88776002: Hereditary factor V deficiency disease (disorder)

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

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

Descriptions:

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

Expanded Value Set

This concept is not in any reference sets

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