autosomaal dominante hereditaire aandoening
hereditaire elliptocytose
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hereditaire elliptocytose door defect in bètaspectrine-zelfassociatie (aandoening)
hereditaire elliptocytose door defect in bètaspectrine-zelfassociatie
HE door defect in bètaspectrine-zelfassociatie
erfelijke ovalocytose door defect in bètaspectrine-zelfassociatie
Hereditary elliptocytosis due to beta spectrin defect in self-association
Id73073009
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