|
deficiëntie van N-carbamoyl-bèta-alanineamidohydrolase (aandoening)
deficiëntie van N-carbamoyl-bèta-alanineamidohydrolase
deficiëntie van bèta-ureidopropionase
Deficiency of beta-ureidopropionase
Id124511000
StatusPrimitive
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetE79.8
TermOverige gespecificeerde stoornissen van purine- en pyrimidinemetabolisme
SNOMED CT to Orphanet simple map65287
SNOMED CT to ICD-10 extended map
TargetE88.8
RuleTRUE
AdviceALWAYS E88.8 | POSSIBLE REQUIREMENT FOR AN EXTERNAL CAUSE CODE
CorrelationSNOMED CT source code to target map code correlation not specified