Autosomal recessive hereditary disorder
Enzymopathy
Hyperprolinemia
Inborn error of metabolism
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Proline dehydrogenase deficiency (disorder)
Proline dehydrogenase deficiency
Proline oxidase deficiency
Hyperprolinemia type I
Hyperprolinemia, type I
hyperprolinemie type 1
Id61071003
StatusPrimitive
OccurrenceCongenital
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetE72.5
RuleTRUE
AdviceALWAYS E72.5
CorrelationSNOMED CT source code to target map code correlation not specified