95842004: Autosomal dominant deficiency of plasminogen (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)\Hereditary hypoplasminogenemia\Autosomal dominant deficiency of plasminogen

\Disease\Genetic disease\Hereditary disease\Hereditary hypoplasminogenemia\Autosomal dominant deficiency of plasminogen
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant deficiency of plasminogen
\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)\Hereditary hypoplasminogenemia\Autosomal dominant deficiency of plasminogen

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Autosomal dominant deficiency of plasminogen	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal dominant deficiency of plasminogen	Is a	Hereditary hypoplasminogenemia	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal dominant deficiency of plasminogen	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal dominant deficiency of plasminogen	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal dominant deficiency of plasminogen	Has definitional manifestation	Hemostatic system finding (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal dominant deficiency of plasminogen	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Autosomal dominant deficiency of plasminogen	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
158739012	Autosomal dominant deficiency of plasminogen	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
158740014	Autosomal dominant deficiency of profibrinolysin	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
840081011	Autosomal dominant deficiency of plasminogen (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
158739012	Autosomal dominant deficiency of plasminogen	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
158739012	Autosomal dominant deficiency of plasminogen	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
158740014	Autosomal dominant deficiency of profibrinolysin	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
158740014	Autosomal dominant deficiency of profibrinolysin	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
840081011	Autosomal dominant deficiency of plasminogen (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
840081011	Autosomal dominant deficiency of plasminogen (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4734551000241117	déficit en plasminogène, type autosomal dominant	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4734551000241117	déficit en plasminogène, type autosomal dominant	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module