Autosomal recessive hereditary disorder
Disorder of carbohydrate metabolism
Enzymopathy
Hereditary nephropathy
Inborn error of metabolism
Metabolic renal disease
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Primary hyperoxaluria (disorder)
Primary hyperoxaluria
Primary oxalosis
primaire hyperoxalurie
primaire hyperoxalurie
Erfelijke stofwisselingsziekte die ontstaat door een overschot aan oxaalzuur of oxalaten in de urine; deze ziekte kan nierstenen en nierverkalking veroorzaken.
Id17901006
StatusPrimitive
Finding siteKidney structure
OccurrenceCongenital
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
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