439145006: Congenital hypofibrinogenemia (disorder)

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

Status: current, Primitive. Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2789363016	Congenital hypofibrinogenemia (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
2794588013	Congenital hypofibrinogenemia	en	Synonym	Active	Case insensitive	SNOMED CT core
2794589017	Congenital hypofibrinogenaemia	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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