Anemia due to intrinsic red cell abnormality	Autosomal dominant hereditary disorder	Hereditary elliptocytosis
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Hereditary elliptocytosis due to alpha spectrin defect (disorder)
	Hereditary elliptocytosis due to alpha spectrin defect
	hereditaire elliptocytose door defect in alfaspectrine
	erfelijke ovalocytose door defect in alfaspectrine HE door defect in alfaspectrine

Id	8857001
Status	Primitive

Has interpretation	Below reference range
Interprets	Measurement of total hemoglobin concentration

Has interpretation	Below reference range
Interprets	Red blood cell count

Has interpretation	Present
Interprets	Hemolysis

Associated morphology	Elliptocyte
Finding site	Erythrocyte
Occurrence	Congenital
Pathological process	Pathological developmental process

ICD-10 complex map reference set

Target	D58.1
Rule	TRUE
Advice	ALWAYS D58.1
Correlation	SNOMED CT source code to target map code correlation not specified