438827002: hereditaire trombofilische dysfibrinogenemie (aandoening)

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:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary thrombophilic dysfibrinogenemia (disorder)	Is a	Hereditary thrombophilia (disorder)	true	Inferred relationship	Some
Hereditary thrombophilic dysfibrinogenemia (disorder)	Is a	Hereditary dysfibrinogenemia (disorder)	true	Inferred relationship	Some
Hereditary thrombophilic dysfibrinogenemia (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	2
Hereditary thrombophilic dysfibrinogenemia (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Hereditary thrombophilic dysfibrinogenemia (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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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
6497071000146119	hereditaire trombofilische dysfibrinogenemie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6497081000146117	hereditaire trombofilische dysfibrinogenemie (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6497091000146115	erfelijke trombofilische dysfibrinogenemie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)