234457009: Hypofibrinogenemia (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\Hypofibrinogenemia (disorder)

\Coagulation factor deficiency syndrome\Disease that manifests either a quantitative or a qualitative defect of factor I\Hypofibrinogenemia (disorder)

\Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\...

\Fibrinogen abnormality\Hypofibrinogenemia (disorder)

\Coagulation factor deficiency syndrome\Disease that manifests either a quantitative or a qualitative defect of factor I\Hypofibrinogenemia (disorder)

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

351285016 Hypofibrinogenaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

351286015 Hypofibrinogenemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

622779019 Hypofibrinogenemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

351285016 Hypofibrinogenaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

351285016 Hypofibrinogenaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

351286015 Hypofibrinogenemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

351286015 Hypofibrinogenemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

622779019 Hypofibrinogenemia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

622779019 Hypofibrinogenemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

819271000241114 hypofibrinogénémie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

819271000241114 hypofibrinogénémie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Acquired hypofibrinogenemia	Is a	True	Hypofibrinogenemia (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Parturient hemorrhage associated with hypofibrinogenemia	Associated with	False	Hypofibrinogenemia (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Antepartum hemorrhage with hypofibrinogenemia	Associated with	False	Hypofibrinogenemia (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Antepartum hemorrhage with hypofibrinogenemia	Is a	True	Hypofibrinogenemia (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Parturient hemorrhage associated with hypofibrinogenemia	Is a	True	Hypofibrinogenemia (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets