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hemorragische diathese door glycoproteïne VI-deficiëntie (aandoening)
hemorragische diathese door glycoproteïne VI-deficiëntie
verhoogde bloedingsneiging door glycoproteïne VI-deficiëntie
Glycoprotein VI deficiency
Bleeding disorder due to glycoprotein VI deficiency
Bleeding disorder platelet-type 11
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).
Id765977002
StatusPrimitive
Has interpretationafwijkend
Interpretshemostase
SNOMED CT to ICD-10 extended map
TargetD69.8
RuleTRUE
AdviceALWAYS D69.8
CorrelationSNOMED CT source code to target map code correlation not specified