Autosomal recessive hereditary disorder
Disorder of carbohydrate metabolism
Enzymopathy
Hereditary nephropathy
Hyperoxaluria
Inborn error of metabolism
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Primary hyperoxaluria (disorder)
Primary hyperoxaluria
Primary oxalosis
Id17901006
StatusPrimitive
Finding siteKidney structure
OccurrenceCongenital
Global Patient Set
SNOMED CT to Orphanet simple map
International Patient Summary
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetE74.8
TermOverige gespecificeerde stofwisselingsstoornissen van koolhydraten
SNOMED CT to ICD-10 extended map
TargetE74.8
RuleTRUE
AdviceALWAYS E74.8
CorrelationSNOMED CT source code to target map code correlation not specified
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Primary hyperoxaluria type III
Primary hyperoxaluria, type I
Primary hyperoxaluria, type II