439000005: Hyperfibrinogenemia (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Procedure related finding\Evaluation finding\...

\Measurement finding\Finding of substance level (finding)\Finding of protein level (finding)\Fibrinogen in blood above reference range\Hyperfibrinogenemia (disorder)
\Measurement finding\Measurement finding outside reference range\Measurement finding above reference range (finding)\Fibrinogen in blood above reference range\Hyperfibrinogenemia (disorder)

\Haematopoietic system finding\Hemostatic system finding (finding)\Fibrinogen in blood above reference range\Hyperfibrinogenemia (disorder)

\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\Hyperfibrinogenemia (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\Hyperfibrinogenemia (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2789153017 Hyperfibrinogenemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2793786017 Hyperfibrinogenaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2795467014 Hyperfibrinogenemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2789153017 Hyperfibrinogenemia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2789153017 Hyperfibrinogenemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2793786017 Hyperfibrinogenaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2793786017 Hyperfibrinogenaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2795467014 Hyperfibrinogenemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2795467014 Hyperfibrinogenemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5326881000241111 hyperfibrinogénémie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5326881000241111 hyperfibrinogénémie 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
Hyperfibrinogenemia (disorder)	Is a	Fibrinogen abnormality	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperfibrinogenemia (disorder)	Has definitional manifestation	Fibrinogen in blood above reference range	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperfibrinogenemia (disorder)	Has interpretation	Above reference range	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hyperfibrinogenemia (disorder)	Is a	Fibrinogen in blood above reference range	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperfibrinogenemia (disorder)	Interprets	Fibrinogen measurement	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hyperfibrinogenemia (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hyperfibrinogenemia (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hyperfibrinogenemia (disorder)	Interprets	Fibrinogen assay, quantitative	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary hyperfibrinogenemia	Is a	True	Hyperfibrinogenemia (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets