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peroxisomale biogenesestoornis door PEX10-mutatie (aandoening)
peroxisomale biogenesestoornis door PEX10-mutatie
peroxisoombiogenesedefect door PEX10-mutatie
stoornis in biogenese van peroxisomen door PEX10-mutatie
PEX10-deficiƫntie
PEX10 deficiency
Peroxisome biogenesis disorder due to PEX10 mutation
Id1187529000
StatusPrimitive
Occurrencecongenitaal
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetE80.3
TermKatalase- en peroxidasedefecten
SNOMED CT to Orphanet simple map247815
SNOMED CT to ICD-10 extended map
TargetQ87.8
RuleTRUE
AdviceALWAYS Q87.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified