Anemia due to intrinsic red cell abnormality
Hereditary elliptocytosis
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Hereditary elliptocytosis due to glycophorin C deficiency (disorder)
Hereditary elliptocytosis due to glycophorin C deficiency
hereditaire elliptocytose door deficiëntie van glycoforine C
erfelijke elliptocytose door glycoforine C-deficiëntie
HE door glycoforine C-deficiëntie
Id15121005
StatusPrimitive
Has interpretationBelow reference range
InterpretsMeasurement of total hemoglobin concentration
Has interpretationBelow reference range
InterpretsRed blood cell count
Has interpretationPresent
InterpretsHemolysis
Associated morphologyElliptocyte
Finding siteErythrocyte
OccurrenceCongenital
Pathological processPathological developmental process
ICD-10 complex map reference set
TargetD58.1
RuleTRUE
AdviceALWAYS D58.1
CorrelationSNOMED CT source code to target map code correlation not specified