Autosomal recessive hereditary disorder
Carbohydrate-deficient glycoprotein syndrome type I
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Congenital disorder of glycosylation type 1w (disorder)
Congenital disorder of glycosylation type 1w
Congenital disorder of glycosylation type Iw
STT3A-CDG (congenital disorder of glycosylation)
A form of congenital disorders of N-linked glycosylation with characteristics of developmental delay, intellectual disability, failure to thrive, hypotonia and seizures. Caused by mutations in the gene STT3A (11q23.3).
congenitaal defect in glycosylering type Iw
CDG-syndroom type Iw
Id733111000
StatusPrimitive
OccurrenceCongenital
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetE77.8
RuleTRUE
AdviceALWAYS E77.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified