439458000: Factor I deficiency disease (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.\Coagulation factor deficiency syndrome\Disease that manifests either a quantitative or a qualitative defect of factor I

\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

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

2788203011 Factor I deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2792737011 Factor I deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2884951017 Disease that manifests either a quantitative or a qualitative defect of factor I en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

2788203011 Factor I deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2792737011 Factor I deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2884951017 Disease that manifests either a quantitative or a qualitative defect of factor I en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

6177291000241117 maladie par déficit en fibrinogène fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6177301000241118 maladie par déficit en facteur I de la coagulation fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6177291000241117 maladie par déficit en fibrinogène fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6177301000241118 maladie par déficit en facteur I de la coagulation 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
Disease that manifests either a quantitative or a qualitative defect of factor I	Is a	Coagulation factor deficiency syndrome	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Disease that manifests either a quantitative or a qualitative defect of factor I	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Disease that manifests either a quantitative or a qualitative defect of factor I	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hypofibrinogenemia (disorder)	Is a	True	Disease that manifests either a quantitative or a qualitative defect of factor I	Inferred relationship	Existential restriction modifier (core metadata concept)
Dysfibrinogenemia	Is a	True	Disease that manifests either a quantitative or a qualitative defect of factor I	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary factor I deficiency disease	Is a	True	Disease that manifests either a quantitative or a qualitative defect of factor I	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets