||
congenitaal defect in glycosylering type 1A (aandoening)
congenitaal defect in glycosylering type 1A
congenital disorder of glycosylation type 1a
fosfomannomutase-2-deficiƫntie
Congenital disorder of glycosylation type Ia
Id459063003
StatusPrimitive
Occurrencecongenitaal
DHD Diagnosethesaurus-referentieset
referentieset met complexe 'mapping' naar ICD-10
TargetE77.8
RuleTRUE
AdviceALWAYS E77.8
CorrelationSNOMED CT source code to target map code correlation not specified