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Severe hereditary spherocytosis due to spectrin deficiency (disorder)
Severe hereditary spherocytosis due to spectrin deficiency
ernstige hereditaire sferocytose door spectrinedeficiƫntie
ernstige erfelijke sferocytose door spectrinedeficiƫntie
ernstige erfelijke sferocytose door deficiƫntie van spectrine
Id77413008
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