111589005: Dysfibrinogenemia (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\Dysfibrinogenemia

\Coagulation factor deficiency syndrome\Disease that manifests either a quantitative or a qualitative defect of factor I\Dysfibrinogenemia

\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital fibrinogen abnormality\Dysfibrinogenemia
\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\Dysfibrinogenemia
\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\Dysfibrinogenemia

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Dysfibrinogenemia	Is a	Congenital fibrinogen abnormality	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Dysfibrinogenemia	Is a	Coagulation factor deficiency syndrome	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Dysfibrinogenemia	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Dysfibrinogenemia	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Dysfibrinogenemia	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Dysfibrinogenemia	Has definitional manifestation	Hemostatic system finding (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Dysfibrinogenemia	Is a	Disease that manifests either a quantitative or a qualitative defect of factor I	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Dysfibrinogenemia	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Dysfibrinogenemia	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Alpha chain defect dysfibrinogenemia	Is a	True	Dysfibrinogenemia	Inferred relationship	Existential restriction modifier (core metadata concept)
Beta chain defect dysfibrinogenaemia	Is a	True	Dysfibrinogenemia	Inferred relationship	Existential restriction modifier (core metadata concept)
Gamma chain defect dysfibrinogenemia	Is a	True	Dysfibrinogenemia	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary dysfibrinogenemia	Is a	True	Dysfibrinogenemia	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
178844010	Dysfibrinogenemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
363901010	Dysfibrinogenaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
632834017	Dysfibrinogenemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
178844010	Dysfibrinogenemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
178844010	Dysfibrinogenemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
363901010	Dysfibrinogenaemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
363901010	Dysfibrinogenaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
632834017	Dysfibrinogenemia (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
632834017	Dysfibrinogenemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
817081000241112	dysfibrinogénémie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
817081000241112	dysfibrinogénémie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module