45366001: Hereditary dysfibrinogenemia (disorder)

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

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
75627010	Congenital dysfibrinogenemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
75628017	Congenital dysfibrinogenemia, NOS	en	Synonym	Inactive	Only initial character case insensitive	SNOMED CT core module
494185015	Congenital dysfibrinogenaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
782597019	Congenital dysfibrinogenemia (disorder)	en	Fully specified name	Inactive	Only initial character case insensitive	SNOMED CT core module
2786838014	Hereditary dysfibrinogenemia (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
2792832010	Hereditary dysfibrinogenaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
2795322018	Hereditary dysfibrinogenemia	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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