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congenitaal defect in glycosylering type 1A (aandoening)
congenitaal defect in glycosylering type 1A
fosfomannomutase-2-deficiëntie
congenital disorder of glycosylation type 1a
Congenital disorder of glycosylation type Ia
Id459063003
StatusPrimitive
Occurrencecongenitaal
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetE77.8
TermOverige gespecificeerde stoornissen van glycoproteïnemetabolisme
SNOMED CT to Orphanet simple map79318
SNOMED CT to ICD-10 extended map
TargetE77.8
RuleTRUE
AdviceALWAYS E77.8
CorrelationSNOMED CT source code to target map code correlation not specified