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Classical phenylketonuria with total deficiency of phenylalanine hydroxylase (disorder)
Classical phenylketonuria with total deficiency of phenylalanine hydroxylase
klassieke fenylketonurie met totale deficiƫntie van fenylalaninehydroxylase
klassieke PKU met volledige deficiƫntie van fenylalaninehydroxylase
Id890436003
StatusPrimitive
OccurrenceCongenital
ICD-10 complex map reference set
TargetE70.0
RuleTRUE
AdviceALWAYS E70.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified