95842004: Autosomal dominant deficiency of plasminogen (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of haemostatic system\Blood coagulation disorder\Disorder involving the fibrinolytic system\Fibrinolytic bleeding syndrome\Hypoplasminogenaemia\Hereditary hypoplasminogenaemia\Autosomal dominant deficiency of plasminogen
• \Disease\Genetic disease\Hereditary disease\Hereditary hypoplasminogenaemia\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 haemostatic system\Blood coagulation disorder\Disorder involving the fibrinolytic system\Fibrinolytic bleeding syndrome\Hypoplasminogenaemia\Hereditary hypoplasminogenaemia\Autosomal dominant deficiency of plasminogen

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
158739012	Autosomal dominant deficiency of plasminogen	en	Synonym	Active	Case insensitive	SNOMED CT core
158740014	Autosomal dominant deficiency of profibrinolysin	en	Synonym	Active	Case insensitive	SNOMED CT core
840081011	Autosomal dominant deficiency of plasminogen (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start