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Peroxisome biogenesis disorder due to PEX13 mutation (disorder)
PEX13 deficiency
Peroxisome biogenesis disorder due to PEX13 mutation
peroxisomale biogenesestoornis door PEX13-mutatie
peroxisoombiogenesedefect door PEX13-mutatie
PEX13-deficiƫntie
stoornis in biogenese van peroxisomen door PEX13-mutatie
Id1187527003
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