autosomaal recessieve hereditaire aandoening
congenitaal defect in glycosylering type I
||
congenitaal defect in glycosylering type 1g (aandoening)
congenitaal defect in glycosylering type 1g
ALG-12-CDG
congenital disorder of glycosylation type 1g
ALG12-congenital disorder of glycosylation
Congenital disorder of glycosylation type Ig
Congenital disorder of glycosylation type 1G
Id711155008
StatusPrimitive
Occurrencecongenitaal
SNOMED CT to Orphanet simple map
DHD Diagnosis thesaurus reference set
SNOMED CT to ICD-10 extended map
TargetE77.8
RuleTRUE
AdviceALWAYS E77.8
CorrelationSNOMED CT source code to target map code correlation not specified