234475005: Thromboxane generation defect (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of blood, lymphatics and immune system\Blood disease\...
• \Hereditary disorder of cellular element of blood\Inherited platelet disorder\Thromboxane generation defect
• \Platelet disorder\Inherited platelet disorder\Thromboxane generation defect
• \Functional finding\Disorder of haemostatic system\Platelet disorder\Inherited platelet disorder\Thromboxane generation defect
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Thromboxane generation defect
• \Disease\Blood disease\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Thromboxane generation defect
• \Disease\Blood disease\Platelet disorder\Inherited platelet disorder\Thromboxane generation defect
• \Disease\Disorder of haemostatic system\Platelet disorder\Inherited platelet disorder\Thromboxane generation defect
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Thromboxane generation defect

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
351309014	Thromboxane generation defect	en	Synonym	Active	Case insensitive	SNOMED CT core
622800012	Thromboxane generation defect (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

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