438827002: Hereditary thrombophilic dysfibrinogenemia (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Functional finding\Disorder of hemostatic system\...
• \Thrombophilia\Hereditary thrombophilia (disorder)\Hereditary thrombophilic dysfibrinogenemia (disorder)
• \Blood coagulation disorder\Fibrinogen abnormality\Congenital fibrinogen abnormality\Dysfibrinogenemia\Hereditary dysfibrinogenemia (disorder)\Hereditary thrombophilic dysfibrinogenemia (disorder)
• \Blood coagulation disorder\Fibrinogen abnormality\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Hereditary dysfibrinogenemia (disorder)\Hereditary thrombophilic dysfibrinogenemia (disorder)
• \Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor I deficiency disease (disorder)\Dysfibrinogenemia\Hereditary dysfibrinogenemia (disorder)\Hereditary thrombophilic dysfibrinogenemia (disorder)
• \Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Hereditary dysfibrinogenemia (disorder)\Hereditary thrombophilic dysfibrinogenemia (disorder)
• \Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia (disorder)\Hereditary thrombophilic dysfibrinogenemia (disorder)
• \Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Hereditary dysfibrinogenemia (disorder)\Hereditary thrombophilic dysfibrinogenemia (disorder)
• \Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital fibrinogen abnormality\Dysfibrinogenemia\Hereditary dysfibrinogenemia (disorder)\Hereditary thrombophilic dysfibrinogenemia (disorder)
• \Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Hereditary dysfibrinogenemia (disorder)\Hereditary thrombophilic dysfibrinogenemia (disorder)
• \Disease\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia (disorder)\Hereditary thrombophilic dysfibrinogenemia (disorder)
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Fibrinogen abnormality\Congenital fibrinogen abnormality\Dysfibrinogenemia\Hereditary dysfibrinogenemia (disorder)\Hereditary thrombophilic dysfibrinogenemia (disorder)
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Fibrinogen abnormality\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Hereditary dysfibrinogenemia (disorder)\Hereditary thrombophilic dysfibrinogenemia (disorder)
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor I deficiency disease (disorder)\Dysfibrinogenemia\Hereditary dysfibrinogenemia (disorder)\Hereditary thrombophilic dysfibrinogenemia (disorder)
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Hereditary dysfibrinogenemia (disorder)\Hereditary thrombophilic dysfibrinogenemia (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Apr 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2786839018	Hereditary thrombophilic dysfibrinogenemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2792833017	Hereditary thrombophilic dysfibrinogenaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2794775012	Hereditary thrombophilic dysfibrinogenemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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