48976006: Prekallikrein 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.\...

\Contact factor deficiency (disorder)\Prekallikrein deficiency

\Coagulation factor deficiency syndrome\Prekallikrein deficiency

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

\Contact factor deficiency (disorder)\Prekallikrein deficiency

\Coagulation factor deficiency syndrome\Prekallikrein deficiency

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

81593014 Prekallikrein deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

81594015 Fletcher factor deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

786603018 Prekallikrein deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1230668019 Fletcher trait en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

81593014 Prekallikrein deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

81593014 Prekallikrein deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

81594015 Fletcher factor deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

786603018 Prekallikrein deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

786603018 Prekallikrein deficiency (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

786603018 Prekallikrein deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1230668019 Fletcher trait en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1230668019 Fletcher trait en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

652081000274111 Präkallikrein-Mangel de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4549811000241116 déficit en prékallikréine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4549811000241116 déficit en prékallikréine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

652081000274111 Präkallikrein-Mangel de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3441521001000111 Präkallikrein-Mangel, kongenitaler de 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
Prekallikrein deficiency	Is a	Contact factor deficiency (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Prekallikrein deficiency	Is a	Coagulation factor deficiency syndrome	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Prekallikrein deficiency	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Prekallikrein deficiency	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Prekallikrein deficiency	Has definitional manifestation	Hemostatic system finding (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Prekallikrein deficiency	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Prekallikrein deficiency	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Acquired prekallikrein deficiency	Is a	True	Prekallikrein deficiency	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary congenital prekallikrein deficiency (disorder)	Is a	True	Prekallikrein deficiency	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets