765977002: Bleeding disorder due to glycoprotein VI 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\Platelet membrane defect\Bleeding disorder due to glycoprotein VI deficiency
• \Platelet disorder\Inherited platelet disorder\Platelet membrane defect\Bleeding disorder due to glycoprotein VI deficiency
• \Functional finding\Disorder of haemostatic system\Platelet disorder\Inherited platelet disorder\Platelet membrane defect\Bleeding disorder due to glycoprotein VI deficiency
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Platelet membrane defect\Bleeding disorder due to glycoprotein VI deficiency
• \Disease\Blood disease\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Platelet membrane defect\Bleeding disorder due to glycoprotein VI deficiency
• \Disease\Blood disease\Platelet disorder\Inherited platelet disorder\Platelet membrane defect\Bleeding disorder due to glycoprotein VI deficiency
• \Disease\Disorder of haemostatic system\Platelet disorder\Inherited platelet disorder\Platelet membrane defect\Bleeding disorder due to glycoprotein VI deficiency
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Platelet membrane defect\Bleeding disorder due to glycoprotein VI deficiency

Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3660331010	Bleeding disorder due to glycoprotein VI deficiency (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3660332015	Bleeding disorder due to glycoprotein VI deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3660333013	Glycoprotein VI deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3660335018	Bleeding disorder platelet-type 11	en	Synonym	Active	Case insensitive	SNOMED CT core
3660334019	A bleeding disorder associated with a decreased ability to form blood clots resulting in increased risk of epistaxis, heavy or prolonged bleeding following minor injury or surgery, ecchymosis and menorrhagia. The disease can be caused by mutations in the GP6 gene, leading to the production of no glycoprotein VI (GPVI) protein, an abnormally short, nonfunctional GPVI protein; or a protein that is less able to bind to collagen. Without GPVI binding to collagen, platelets cannot come together efficiently to form a clot. The disease may also be acquired rather than inherited and such cases are associated with autoimmune disorders such as systemic lupus erythematosus (SLE).	en	Definition	Active	Case sensitive	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