peroxisomale biogenesestoornis
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peroxisomale biogenesestoornis door PEX2-mutatie (aandoening)
peroxisomale biogenesestoornis door PEX2-mutatie
peroxisoombiogenesedefect door PEX2-mutatie
PEX2-deficiëntie
stoornis in biogenese van peroxisomen door PEX2-mutatie
PEX2 deficiency
Peroxisome biogenesis disorder due to PEX2 mutation
Id1187525006
StatusPrimitive
Occurrencecongenitaal
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