95842004: autosomaal dominante plasminogeendeficiëntie (aandoening)

SNOMED CT Concept\Clinical finding (finding)\...

\Functional finding\Disorder of hemostatic system\Blood coagulation disorder\Disorder involving the fibrinolytic system\Fibrinolytic bleeding syndrome\Hypoplasminogenaemia\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\Blood coagulation disorder\Disorder involving the fibrinolytic system\Fibrinolytic bleeding syndrome\Hypoplasminogenaemia\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:

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

6328201000146116 autosomaal dominante deficiëntie van profibrinolysine nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6328211000146119 autosomaal dominante plasminogeendeficiëntie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6328221000146112 autosomaal dominante plasminogeendeficiëntie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

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	Some
Autosomal dominant deficiency of plasminogen	Is a	Hereditary hypoplasminogenemia	true	Inferred relationship	Some
Autosomal dominant deficiency of plasminogen	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Some
Autosomal dominant deficiency of plasminogen	Finding site	Body system structure	false	Inferred relationship	Some
Autosomal dominant deficiency of plasminogen	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
Autosomal dominant deficiency of plasminogen	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Autosomal dominant deficiency of plasminogen	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets