Autosomal recessive hereditary disorder
Carbohydrate-deficient glycoprotein syndrome type I
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ALG12-congenital disorder of glycosylation (disorder)
ALG12-congenital disorder of glycosylation
Congenital disorder of glycosylation type Ig
Congenital disorder of glycosylation type 1G
congenitaal defect in glycosylering type 1g
ALG-12-CDG
congenital disorder of glycosylation type 1g
Id711155008
StatusPrimitive
OccurrenceCongenital
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetE77.8
RuleTRUE
AdviceALWAYS E77.8
CorrelationSNOMED CT source code to target map code correlation not specified