Anemia due to intrinsic red cell abnormality
Autosomal dominant hereditary disorder
Hereditary elliptocytosis
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Hereditary elliptocytosis due to abnormal protein 4.1 (disorder)
Hereditary elliptocytosis due to abnormal protein 4.1
hereditaire elliptocytose door afwijkend eiwit 4.1
erfelijke ovalocytose door abnormaal proteïne 4.1
HE door afwijkend eiwit 4.1
Id75443009
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