|
Peroxisome biogenesis disorder due to PEX3 mutation (disorder)
PEX3 deficiency
Peroxisome biogenesis disorder due to PEX3 mutation
peroxisomale biogenesestoornis door PEX3-mutatie
PEX3-deficiƫntie
stoornis in biogenese van peroxisomen door PEX3-mutatie
peroxisoombiogenesedefect door PEX3-mutatie
Id1187523004
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