95840007: Hypoplasminogenemia (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.\Disorder involving the fibrinolytic system\Fibrinolytic bleeding syndrome\Hypoplasminogenemia (disorder)

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

158735018 Hypoplasminogenemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

512322011 Plasminogen deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

512323018 Hypoplasminogenaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

840078018 Hypoplasminogenemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

158735018 Hypoplasminogenemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

158735018 Hypoplasminogenemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

512322011 Plasminogen deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

512322011 Plasminogen deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

512323018 Hypoplasminogenaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

512323018 Hypoplasminogenaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

840078018 Hypoplasminogenemia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

840078018 Hypoplasminogenemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3381381001000118 Hypoplasminogenämie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

890751000172111 déficit en plasminogène type 1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

944641000172113 déficit congénital en plasminogène fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

890751000172111 déficit en plasminogène type 1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

944641000172113 déficit congénital en plasminogène fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3381381001000118 Hypoplasminogenämie 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
Hypoplasminogenemia (disorder)	Is a	Fibrinolytic bleeding syndrome	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hypoplasminogenemia (disorder)	Is a	Disorder involving the fibrinolytic system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hypoplasminogenemia (disorder)	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hypoplasminogenemia (disorder)	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hypoplasminogenemia (disorder)	Has definitional manifestation	Hemostatic system finding (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hypoplasminogenemia (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hypoplasminogenemia (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary hypoplasminogenemia	Is a	True	Hypoplasminogenemia (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Acquired hypoplasminogenaemia	Is a	True	Hypoplasminogenemia (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets