95842004: Autosomal dominant deficiency of plasminogen (disorder)

• SNOMED CT Concept\constatation clinique\...
• \constatation fonctionnelle\Disorder of haemostatic system\Blood coagulation disorder\Disorder involving the fibrinolytic system\Fibrinolytic bleeding syndrome\Hypoplasminogenemia\Hereditary hypoplasminogenemia\Autosomal dominant deficiency of plasminogen
• \Disease\Genetic disease\maladie héréditaire\Hereditary hypoplasminogenemia\Autosomal dominant deficiency of plasminogen
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant deficiency of plasminogen
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Disorder involving the fibrinolytic system\Fibrinolytic bleeding syndrome\Hypoplasminogenemia\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

Expanded Value Set

This concept is not in any reference sets

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