45366001: Hereditary dysfibrinogenemia (disorder)

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

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2786838014	Hereditary dysfibrinogenemia (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
2792832010	Hereditary dysfibrinogenaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
2795322018	Hereditary dysfibrinogenemia	en	Synonym	Active	Case insensitive	SNOMED CT core
494185015	Congenital dysfibrinogenaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
75627010	Congenital dysfibrinogenemia	en	Synonym	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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