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neonataal antifosfolipidesyndroom (aandoening)
neonataal antifosfolipidesyndroom
neonataal APS
Neonatal antiphospholipid syndrome
Neonatal Hughes syndrome
Neonatal antiphospholipid antibody syndrome
A rare secondary neonatal autoimmune disease with characteristics of single or recurrent episodes of venous, arterial or mixed thrombosis in a neonate whose mother does not have antiphospholipid syndrome manifestations. Patients present positive antiphospholipid antibodies and may have additional abnormalities associated (for example cardiac valve disease, livedo reticularis, thrombocytopenia, nephropathy, neurological manifestations).
Id774084003
StatusDefined
Causative agentAnti-phospholipid antibody
Occurrenceneonataal
Pathological processauto-immuunproces
Has interpretationafwijkend
Interpretshemostase
referentieset met complexe 'mapping' naar ICD-10
TargetD68.6
RuleTRUE
AdviceALWAYS D68.6 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified