234471001: Glycoprotein Ia 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\Platelet membrane defect\Glycoprotein Ia defect
• \Platelet disorder\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ia defect
• \Functional finding\Disorder of haemostatic system\Platelet disorder\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ia defect
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ia defect
• \Disease\Blood disease\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ia defect
• \Disease\Blood disease\Platelet disorder\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ia defect
• \Disease\Disorder of haemostatic system\Platelet disorder\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ia defect
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ia defect

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
351304016	Glycoprotein Ia defect	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
622795019	Glycoprotein Ia defect (disorder)	en	Fully specified name	Active	Initial character 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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