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primaire CD59-deficiƫntie (aandoening)
primaire CD59-deficiƫntie
Primary CD59 deficiency
A rare genetic hematologic and neurologic disease characterized by chronic Coombs-negative hemolysis. The disease is associated with early-onset relapsing immune-mediated inflammatory axonal or demyelinating sensory-motor peripheral polyneuropathy and isolated or recurrent cerebrovascular events (in anterior or posterior circulation).
Id778027003
StatusPrimitive
Finding siteerytrocyt
Has interpretationaanwezig
Interpretshemolyse
Pathological processafwijkend immuunproces
referentieset met complexe 'mapping' naar ICD-10
TargetD84.1
RuleTRUE
AdviceALWAYS D84.1
CorrelationSNOMED CT source code to target map code correlation not specified