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438827002: Hereditary thrombophilic dysfibrinogenemia (disorder)

SNOMED CT Concept\Clinical finding\...

\Functional finding\Disorder of hemostatic system\...

\Thrombophilia\Hereditary thrombophilia\Hereditary thrombophilic dysfibrinogenemia

\Blood coagulation disorder\Fibrinogen abnormality\Congenital fibrinogen abnormality\Dysfibrinogenemia\Hereditary dysfibrinogenemia\Hereditary thrombophilic dysfibrinogenemia
\Blood coagulation disorder\Fibrinogen abnormality\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Hereditary dysfibrinogenemia\Hereditary thrombophilic dysfibrinogenemia
\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor I deficiency disease\Dysfibrinogenemia\Hereditary dysfibrinogenemia\Hereditary thrombophilic dysfibrinogenemia
\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Hereditary dysfibrinogenemia\Hereditary thrombophilic dysfibrinogenemia

\Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia\Hereditary thrombophilic dysfibrinogenemia
\Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Hereditary dysfibrinogenemia\Hereditary thrombophilic dysfibrinogenemia
\Disease\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia\Hereditary thrombophilic dysfibrinogenemia
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Fibrinogen abnormality\Congenital fibrinogen abnormality\Dysfibrinogenemia\Hereditary dysfibrinogenemia\Hereditary thrombophilic dysfibrinogenemia
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Fibrinogen abnormality\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Hereditary dysfibrinogenemia\Hereditary thrombophilic dysfibrinogenemia
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor I deficiency disease\Dysfibrinogenemia\Hereditary dysfibrinogenemia\Hereditary thrombophilic dysfibrinogenemia
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Hereditary dysfibrinogenemia\Hereditary thrombophilic dysfibrinogenemia
\Disease\Congenital disease\Congenital fibrinogen abnormality\Dysfibrinogenemia\Hereditary dysfibrinogenemia\Hereditary thrombophilic dysfibrinogenemia
\Disease\Congenital disease\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Hereditary dysfibrinogenemia\Hereditary thrombophilic dysfibrinogenemia

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

Descriptions:

Id Description Lang Type Status Case? Module

2786839018 Hereditary thrombophilic dysfibrinogenemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

2792833017 Hereditary thrombophilic dysfibrinogenaemia en Synonym Active Entire term case insensitive SNOMED CT core module

2794775012 Hereditary thrombophilic dysfibrinogenemia en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary thrombophilic dysfibrinogenemia	Is a	Hereditary thrombophilia	true	Inferred relationship	Existential restriction modifier
Hereditary thrombophilic dysfibrinogenemia	Is a	Hereditary dysfibrinogenemia	true	Inferred relationship	Existential restriction modifier
Hereditary thrombophilic dysfibrinogenemia	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Hereditary thrombophilic dysfibrinogenemia	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier	1
Hereditary thrombophilic dysfibrinogenemia	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier	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	SNOMED CT core module
2792833017	Hereditary thrombophilic dysfibrinogenaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
2794775012	Hereditary thrombophilic dysfibrinogenemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module