familiaire aandoening
hemolytisch-uremisch syndroom
||
familiair hemolytisch-uremisch syndroom (aandoening)
familiair hemolytisch-uremisch syndroom
familiair HUS
Familial hemolytic uremic syndrome
Hemolytic uremic syndrome with either a family history of hemolytic uremic syndrome or a genetic mutation known to cause hemolytic uremic syndrome, or both.
Id722721004
StatusPrimitive
Clinical courseonverwacht optredend en/of van korte duur
Finding sitestructuur van nier
Has interpretationonder referentiebereik
InterpretsMeasurement of total hemoglobin concentration
Has interpretationonder referentiebereik
Interpretstelling van erytrocyten
Associated morphologyschistocyt
Has interpretationonder referentiebereik
InterpretsPlatelet count
Has interpretationaanwezig
Interpretshemolyse
Finding siteerytrocyt
Has interpretationgestoord
Interpretsnierfunctie
Associated morphologymicrotrombus
Finding sitestructuur van capillair
Associated morphologymicrotrombus
Finding sitestructuur van arteriola
Global Patient Set
SNOMED CT to ICD-10 extended map
TargetD59.3
RuleTRUE
AdviceALWAYS D59.3
CorrelationSNOMED CT source code to target map code correlation not specified