154818001: Congenital afibrinogenemia (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of hemostatic system\Blood coagulation disorder\...
• \Fibrinogen abnormality\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Congenital afibrinogenemia
• \Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Congenital afibrinogenemia
• \Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Congenital afibrinogenemia
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Fibrinogen abnormality\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Congenital afibrinogenemia
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Congenital afibrinogenemia
• \Disease\Congenital disease\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Congenital afibrinogenemia

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2009. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
240815017	Congenital afibrinogenemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
240816016	Congenital afibrinogenaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
2788877018	Congenital afibrinogenemia (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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