234477002: Thromboxane synthetase deficiency (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\Thromboxane synthetase deficiency
• \Platelet disorder\Inherited platelet disorder\Thromboxane generation defect\Thromboxane synthetase deficiency
• \Functional finding\Disorder of haemostatic system\Platelet disorder\Inherited platelet disorder\Thromboxane generation defect\Thromboxane synthetase deficiency
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Thromboxane generation defect\Thromboxane synthetase deficiency
• \Disease\Blood disease\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Thromboxane generation defect\Thromboxane synthetase deficiency
• \Disease\Blood disease\Platelet disorder\Inherited platelet disorder\Thromboxane generation defect\Thromboxane synthetase deficiency
• \Disease\Disorder of haemostatic system\Platelet disorder\Inherited platelet disorder\Thromboxane generation defect\Thromboxane synthetase deficiency
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Thromboxane generation defect\Thromboxane synthetase deficiency

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
351311017	Thromboxane synthetase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
622802016	Thromboxane synthetase deficiency (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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