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Peroxisome biogenesis disorder due to PEX2 mutation (disorder)
PEX2 deficiency
Peroxisome biogenesis disorder due to PEX2 mutation
peroxisomale biogenesestoornis door PEX2-mutatie
PEX2-deficiƫntie
stoornis in biogenese van peroxisomen door PEX2-mutatie
peroxisoombiogenesedefect door PEX2-mutatie
Id1187525006
StatusPrimitive
OccurrenceCongenital
ICD-10 complex map reference set
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