Autosomal recessive hereditary disorder	Hereditary persistence of fetal hemoglobin	Sickling disorder due to hemoglobin S
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Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome (disorder)
	Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome
	A rare genetic hemoglobinopathy characterized by generally mild clinical phenotype, high fetal hemoglobin levels and mild microcytosis and hypochromia. In some cases, acute sickle cell disease manifestations were reported, namely acute chest syndrome and acute pain crisis.
	syndroom van hereditaire persistentie van foetaal hemoglobine met sikkelcelziekte
	syndroom van erfelijke persistentie van foetaal hemoglobine met sikkelcelziekte syndroom van HPFH met sikkelcelziekte syndroom van hereditaire persistentie van HbF met sikkelcelziekte

Id	783254003
Status	Primitive

Finding site	Erythrocyte
Occurrence	Congenital

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	D56.4
Rule	TRUE
Advice	ALWAYS D56.4
Correlation	SNOMED CT source code to target map code correlation not specified

Target	D57.2
Rule	TRUE
Advice	ALWAYS D57.2
Correlation	SNOMED CT source code to target map code correlation not specified