autosomaal recessieve hereditaire aandoening
congenitale immunodeficiëntie
congenitale trombocytopenie
gecombineerde immunodeficiëntie
hereditaire aandoening van immuunsysteem
hereditaire trombocytopenie
immuuntrombocytopenie
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Autosomal recessive combined immunodeficiency due to Arp2/3-mediated filament branching defect (disorder)
Autosomal recessive combined immunodeficiency due to Arp2/3-mediated filament branching defect
Autosomal recessive combined immunodeficiency due to ARPC1B mutation
Id1351778007
StatusPrimitive
Occurrencecongenitaal
Finding sitestructuur van lichaamssysteem
Pathological processafwijkend immuunproces
Has interpretationafwijkend
Interpretshemostase
Has interpretationonder referentiebereik
InterpretsPlatelet count
SNOMED CT to ICD-10 extended map
TargetD81.8
RuleTRUE
AdviceALWAYS D81.8
CorrelationSNOMED CT source code to target map code correlation not specified