peroxisomale biogenesestoornis
|
peroxisomale biogenesestoornis door PEX16-mutatie (aandoening)
peroxisomale biogenesestoornis door PEX16-mutatie
stoornis in biogenese van peroxisomen door PEX16-mutatie
peroxisoombiogenesedefect door PEX16-mutatie
PEX16-deficiëntie
PEX16 deficiency
Peroxisome biogenesis disorder due to PEX16 mutation
Id1187526007
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