anemie door intrinsieke afwijking van erytrocyt
autosomaal dominante hereditaire aandoening
hereditaire elliptocytose
|||
hereditaire elliptocytose door defect in alfaspectrine (aandoening)
hereditaire elliptocytose door defect in alfaspectrine
erfelijke ovalocytose door defect in alfaspectrine
HE door defect in alfaspectrine
Hereditary elliptocytosis due to alpha spectrin defect
Id8857001
StatusPrimitive
Has interpretationonder referentiebereik
InterpretsMeasurement of total hemoglobin concentration
Has interpretationonder referentiebereik
Interpretstelling van erytrocyten
Has interpretationaanwezig
Interpretshemolyse
Associated morphologyelliptocyt
Finding siteerytrocyt
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
SNOMED CT to ICD-10 extended map
TargetD58.1
RuleTRUE
AdviceALWAYS D58.1
CorrelationSNOMED CT source code to target map code correlation not specified