439145006: Congenital hypofibrinogenemia (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 hypofibrinogenemia
• \Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Congenital hypofibrinogenemia
• \Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Congenital hypofibrinogenemia
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Fibrinogen abnormality\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Congenital hypofibrinogenemia
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Congenital hypofibrinogenemia
• \Disease\Congenital disease\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Congenital hypofibrinogenemia

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
2789363016	Congenital hypofibrinogenemia (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
2794588013	Congenital hypofibrinogenemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
2794589017	Congenital hypofibrinogenaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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