234458004: Hypodysfibrinogenemia (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Functional finding\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\...
• \Fibrinogen abnormality\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Hypodysfibrinogenemia
• \Coagulation factor deficiency syndrome\Disease that manifests either a quantitative or a qualitative defect of factor I\Hereditary factor I deficiency disease\Hypodysfibrinogenemia
• \Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Hypodysfibrinogenemia
• \Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Hypodysfibrinogenemia
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hereditary factor I deficiency disease\Hypodysfibrinogenemia
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Hypodysfibrinogenemia
• \Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Fibrinogen abnormality\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Hypodysfibrinogenemia
• \Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Coagulation factor deficiency syndrome\Disease that manifests either a quantitative or a qualitative defect of factor I\Hereditary factor I deficiency disease\Hypodysfibrinogenemia
• \Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Hypodysfibrinogenemia

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
351287012	Hypodysfibrinogenaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
351288019	Hypodysfibrinogenemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
622781017	Hypodysfibrinogenemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
351287012	Hypodysfibrinogenaemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
351287012	Hypodysfibrinogenaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
351288019	Hypodysfibrinogenemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
351288019	Hypodysfibrinogenemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
622781017	Hypodysfibrinogenemia (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
622781017	Hypodysfibrinogenemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3444301001000113	Hypodysfibrinogenämie, familiäre	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6282191000241118	hypodysfibrinogénémie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6282191000241118	hypodysfibrinogénémie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3444301001000113	Hypodysfibrinogenämie, familiäre	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

This concept is not in any reference sets

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