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Hereditary spherocytosis due to beta spectrin defect (disorder)
Hereditary spherocytosis due to beta spectrin defect
hereditaire sferocytose door defect van bètaspectrine
erfelijke sferocytose door defect van bètaspectrine
congenitale sferocytose door defect van bètaspectrine
Id69981004
StatusPrimitive
Finding siteErythrocyte
Associated morphologySpherocyte
Finding siteHematopoietic system structure
Has interpretationBelow reference range
InterpretsRed blood cell count
Has interpretationPresent
InterpretsHemolysis
ICD-10 complex map reference set
TargetD58.0
RuleTRUE
AdviceALWAYS D58.0
CorrelationSNOMED CT source code to target map code correlation not specified