73975000: Factor II deficiency (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.\...

\Prothrombin complex deficiency\Factor II deficiency (disorder)

\Coagulation factor deficiency syndrome\Factor II deficiency (disorder)

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

\Prothrombin complex deficiency\Factor II deficiency (disorder)

\Coagulation factor deficiency syndrome\Factor II deficiency (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

122845019 Factor II deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

122848017 Prothrombin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

814422014 Factor II deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

122845019 Factor II deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

122845019 Factor II deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

122848017 Prothrombin deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

122848017 Prothrombin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

814422014 Factor II deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

814422014 Factor II deficiency (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

814422014 Factor II deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

6945931000241116 déficit en facteur II fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6945931000241116 déficit en facteur II fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Factor II deficiency (disorder)	Is a	Coagulation factor deficiency syndrome	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Factor II deficiency (disorder)	Is a	Prothrombin complex deficiency	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Factor II deficiency (disorder)	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Factor II deficiency (disorder)	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Factor II deficiency (disorder)	Has definitional manifestation	Hemostatic system finding (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Factor II deficiency (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Factor II deficiency (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Haemorrhagic disease of the newborn due to factor II deficiency	Is a	False	Factor II deficiency (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary factor II deficiency disease (disorder)	Is a	True	Factor II deficiency (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Acquired factor II deficiency	Is a	True	Factor II deficiency (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Haemorrhagic disease of the newborn due to factor II deficiency	Associated etiologic finding	False	Factor II deficiency (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Haemorrhagic disease of the newborn due to factor II deficiency	Due to	True	Factor II deficiency (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)	1

This concept is not in any reference sets