234456000: Congenital fibrinogen abnormality (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

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

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

351284017 Congenital fibrinogen abnormality en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

622778010 Congenital fibrinogen abnormality (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

351284017 Congenital fibrinogen abnormality en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

351284017 Congenital fibrinogen abnormality en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

622778010 Congenital fibrinogen abnormality (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

622778010 Congenital fibrinogen abnormality (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

110621000077110 anomalie congénitale du fibrinogène fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

110621000077110 anomalie congénitale du fibrinogène 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
Congenital fibrinogen abnormality	Is a	Fibrinogen abnormality	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital fibrinogen abnormality	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital fibrinogen abnormality	Is a	Congenital disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital fibrinogen abnormality	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital fibrinogen abnormality	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital fibrinogen abnormality	Has definitional manifestation	Hemostatic system finding (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital fibrinogen abnormality	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital fibrinogen abnormality	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hypofibrinogenemia (disorder)	Is a	False	Congenital fibrinogen abnormality	Inferred relationship	Existential restriction modifier (core metadata concept)
Hypodysfibrinogenemia	Is a	False	Congenital fibrinogen abnormality	Inferred relationship	Existential restriction modifier (core metadata concept)
Dysfibrinogenemia	Is a	True	Congenital fibrinogen abnormality	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary factor I deficiency disease	Is a	True	Congenital fibrinogen abnormality	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets