154818001: Congenital afibrinogenemia (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 afibrinogenaemia
• \Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Congenital afibrinogenaemia
• \Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Congenital afibrinogenaemia
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Fibrinogen abnormality\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Congenital afibrinogenaemia
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Congenital afibrinogenaemia
• \Disease\Congenital disease\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Congenital afibrinogenaemia

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

Descriptions:

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