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